Canonical Allele Identifier: PA2825613900
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 245777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Leu133Pro
CA10584586
NM_001126116.1:c.398T>C
CA645588450
NM_001126116.1:c.398_399delinsCT