Allele Registry

Canonical Allele Identifier: PA162721

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000032137

RCV000122280

ClinVar Variation:

38888

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Arg834Cys	CA162719 NM_000553.6:c.2500C>T