Canonical Allele Identifier: PA658679390
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Cys275Trp
CA397836936
NM_001126114.3:c.825T>G