Canonical Allele Identifier: PA2826567592
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494469
ClinVar RCV Id: RCV001989365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Glu255Ala
CA397836510
NM_001276761.3:c.764A>C