Allele Registry

Canonical Allele Identifier: PA162736

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122285

RCV000227936

RCV000857886

RCV004019696

ClinVar Variation:

135428

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ala995Thr	CA162734 NM_000553.6:c.2983G>A