Allele Registry

Canonical Allele Identifier: PA658664914

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000538283

RCV003153686

ClinVar Variation:

458390

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Asp58Asn	CA4703996 NM_000553.6:c.172G>A