Allele Registry

Canonical Allele Identifier: PA2579952748

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000417693

RCV000418362

RCV000420498

RCV000422668

RCV000423297

RCV000424776

RCV000425100

RCV000425394

RCV000425782

RCV000427544

RCV000427948

RCV000430735

RCV000432207

RCV000432931

RCV000433611

RCV000435050

RCV000435353

RCV000436038

RCV000437882

RCV000440334

RCV000441010

RCV000441711

RCV000444356

RCV000444427

RCV000444519

RCV000626118

RCV000633396

RCV001026425

RCV004022238

ClinVar Variation:

376652

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg248Gly	CA16603069 NM_000546.6:c.742C>G