Canonical Allele Identifier: PA2826563252
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376672
ClinVar RCV Id: RCV000418104 RCV000419558 RCV000418474 RCV000423283 RCV000424832 RCV000429825 RCV000429571 RCV000434860 RCV000436131 RCV000439819 RCV000440944 RCV002356519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Val57Glu
CA16603086
NM_001276698.3:c.170T>A