Canonical Allele Identifier: PA2826565069
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480758
ClinVar RCV Id: RCV000565337
ClinVar Variation Id: 1462102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Gly78Arg
CA397844409
NM_001276760.3:c.232G>C
CA397844412
NM_001276760.3:c.232G>A