Canonical Allele Identifier: PA2826561690
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 132973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.His257Tyr
CA000474
NM_001276696.3:c.769C>T