Canonical Allele Identifier: PA2826564870
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 919370
ClinVar RCV Id: RCV001177508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ala30Pro
CA397845901
NM_001276760.3:c.88G>C