Canonical Allele Identifier: PA2826565557
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2969522
ClinVar RCV Id: RCV003821656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asp168Asn
CA287488336
NM_001276760.3:c.502G>A