Canonical Allele Identifier: PA2579951193
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 234059
ClinVar Variation Id: 2774646
ClinVar RCV Id: RCV003585848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Gly356Arg
CA000803
NM_000546.6:c.1066G>C
CA287485729
NM_000546.6:c.1066G>A