Allele Registry

Canonical Allele Identifier: PA2826563275

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000115731

RCV000213055

RCV000232050

RCV000417417

RCV000418951

RCV000423029

RCV000423111

RCV000423624

RCV000425193

RCV000425869

RCV000428097

RCV000428791

RCV000433936

RCV000434300

RCV000434614

RCV000435063

RCV000436553

RCV000439456

RCV000439645

RCV000440244

RCV000442230

RCV000444717

RCV000444814

RCV000785544

RCV001310212

RCV001527468

RCV001579295

RCV002490776

RCV003162539

RCV003407499

RCV003460829

RCV003997298

ClinVar Variation:

127819

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263627.1:p.Tyr61Cys	CA000315 NM_001276698.3:c.182A>G