Allele Registry

Canonical Allele Identifier: PA162760

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122293

RCV000231281

RCV000858031

ClinVar Variation:

135436

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Thr1262Arg	CA162758 NM_000553.6:c.3785C>G