Allele Registry

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This migration is underway but taking longer than originally estimated.

Canonical Allele Identifier: PA336902

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216473

ClinVar RCV Id: RCV000197011

ClinVar Variation Id: 1047514

ClinVar RCV Id: RCV001352238 RCV002377500

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119587.1:p.Gly170Arg	CA336894 NM_001126115.1:c.508G>C CA397836336 NM_001126115.1:c.508G>A