Canonical Allele Identifier: PA2826563447
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12356
ClinVar RCV Id: RCV000013150 RCV000115736 RCV000148913 RCV000197114 RCV000235221 RCV000417916 RCV000420727 RCV000421194 RCV000426606 RCV000426359 RCV000433424 RCV000432778 RCV000435533 RCV000437518 RCV000437291 RCV000444656 RCV000438410 RCV000439963 RCV000445244 RCV000419135 RCV000420303 RCV000421893 RCV000424869 RCV000427709 RCV000432587 RCV000437935 RCV000426233 RCV000428591 RCV000430513 RCV000441226 RCV000445235 RCV000763417 RCV000790860 RCV000785344 RCV001527465 RCV001255671 RCV001257519 RCV001270275 RCV001789749 RCV001554245 RCV003162244 RCV003332079 RCV003996090 RCV003466852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Arg89Gln
CA000387
NM_001276698.3:c.266G>A
CA645588545
NM_001276698.3:c.266_267delinsAA