Canonical Allele Identifier: PA2826562222
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Tyr77His
CA338059
NM_001276697.3:c.229T>C