Canonical Allele Identifier: PA645436198
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 418517
ClinVar RCV Id: RCV000484792 RCV000551566 RCV001527084 RCV002350050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro58Leu
CA16620625
NM_001126117.1:c.173C>T