Allele Registry

Canonical Allele Identifier: PA156031

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000118880

RCV000273969

RCV000835594

RCV003315695

ClinVar Variation:

130762

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Cys1367Arg	CA156029 NM_000553.6:c.4099T>C