Canonical Allele Identifier: PA2826561019
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 956854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro138His
CA397841407
NM_001276696.3:c.413C>A
CA645588943
NM_001276696.3:c.413_414delinsAT