Allele Registry

Canonical Allele Identifier: PA645437318

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000229198

RCV003153528

RCV003967620

ClinVar Variation:

238139

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Thr781Ile	CA4704724 NM_000553.6:c.2342C>T