Canonical Allele Identifier: PA106709
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12347
ClinVar Variation Id: 437017
ClinVar RCV Id: RCV000499534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Arg248Trp
CA000382
NM_000546.6:c.742C>T
CA645373070
NM_000546.6:c.741_742delinsTT