Canonical Allele Identifier: PA2826567670
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro277Thr
CA001212
NM_001276761.3:c.829C>A