Canonical Allele Identifier: PA122152
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12352
ClinVar Variation Id: 406598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Arg249Ser
CA000392
NM_000546.6:c.747G>T
CA16615944
NM_000546.6:c.747G>C