Allele Registry

Canonical Allele Identifier: PA162712

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122277

RCV000725735

RCV001080213

RCV003398738

ClinVar Variation:

135421

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Arg637Trp	CA162710 NM_000553.6:c.1909C>T