Canonical Allele Identifier: PA2825613095
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 644883
ClinVar RCV Id: RCV000798870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Val71Glu
CA397840380
NM_001126116.1:c.212T>A