Allele Registry

Canonical Allele Identifier: PA2826559887

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418854

RCV000420011

RCV000426368

RCV000427640

RCV000428926

RCV000429581

RCV000436108

RCV000437044

RCV000438332

RCV000438482

RCV000442626

RCV000567507

RCV001851021

RCV002289529

RCV002510885

ClinVar Variation:

376637

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Asn200Ser	CA16603054 NM_001276695.3:c.599A>G CA645588625 NM_001276695.3:c.599_600delinsGT