Allele Registry

Canonical Allele Identifier: PA645437022

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000464118

RCV002510900

ClinVar Variation:

412710

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ser394Leu	CA4704263 NM_000553.6:c.1181C>T