Canonical Allele Identifier: PA2826562065
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Tyr46Cys
CA16603095
NM_001276697.3:c.137A>G