Allele Registry

Canonical Allele Identifier: PA645437223

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000338817

RCV003153566

RCV003168567

ClinVar Variation:

362805

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ile710Val	CA4704653 NM_000553.6:c.2128A>G