Canonical Allele Identifier: PA169987
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Met40Thr
CA000050
NM_001126114.3:c.119T>C