Canonical Allele Identifier: PA106871
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 140801
ClinVar RCV Id: RCV000128975 RCV000417795 RCV000423419 RCV000435449 RCV000427068 RCV000428004 RCV000429076 RCV000436530 RCV000444430 RCV000472876 RCV000418811 RCV000427674 RCV000437920 RCV000439333 RCV000785510 RCV001582600 RCV002288619
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Cys141Tyr
CA000174
NM_000546.6:c.422G>A