Canonical Allele Identifier: PA2825618770
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Cys236Trp
CA397836936
NM_001126118.1:c.708T>G