Canonical Allele Identifier: PA2579935996
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 956854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro177His
CA397841407
NM_000546.6:c.530C>A
CA645588943
NM_000546.6:c.530_531delinsAT