Allele Registry

Canonical Allele Identifier: PA645436831

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000470096

RCV001591059

ClinVar Variation:

404007

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Leu44Val	CA4703988 NM_000553.6:c.130C>G