Canonical Allele Identifier: PA287782
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127819
ClinVar RCV Id: RCV000115731 RCV000213055 RCV000232050 RCV000418951 RCV000423029 RCV000423111 RCV000423624 RCV000425869 RCV000433936 RCV000434300 RCV000435063 RCV000444814 RCV000417417 RCV000428791 RCV000444717 RCV000425193 RCV000439456 RCV000440244 RCV000442230 RCV000785544 RCV001310212 RCV000428097 RCV000434614 RCV000436553 RCV000439645 RCV001579295 RCV003460829 RCV003162539 RCV003407499 RCV003997298 RCV001527468 RCV002490776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Tyr181Cys
CA000315
NM_001126118.1:c.542A>G