Allele Registry

Canonical Allele Identifier: PA1139672064

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV001049557

ClinVar Variation:

846289

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Gln1229Pro	CA4705145 NM_000553.6:c.3686A>C