Canonical Allele Identifier: PA2826559866
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182934
ClinVar RCV Id: RCV000161033 RCV000200500 RCV000421083 RCV000421733 RCV000430423 RCV000431774 RCV000439317 RCV000439996 RCV000419726 RCV000422107 RCV000429307 RCV000434187 RCV000443583 RCV000443569 RCV001526334 RCV002288692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Met198Val
CA000348
NM_001276695.3:c.592A>G