Allele Registry

Canonical Allele Identifier: PA658665004

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000551303

RCV003316686

RCV003942745

ClinVar Variation:

458382

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Asp460Asn	CA4704341 NM_000553.6:c.1378G>A