Canonical Allele Identifier: PA2826566509
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406607
ClinVar RCV Id: RCV000471826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg26Thr
CA16615958
NM_001276761.3:c.77G>C