Canonical Allele Identifier: PA338072
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Tyr236His
CA338059
NM_001126112.3:c.706T>C