Allele Registry

Canonical Allele Identifier: PA2825618382

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417900

RCV000420803

RCV000426704

RCV000427357

RCV000428013

RCV000428578

RCV000435223

RCV000437385

RCV000438030

RCV000442190

RCV000444807

RCV000461418

ClinVar Variation:

376581

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119590.1:p.Cys203Gly	CA501041 NM_001126118.1:c.607T>G