Allele Registry

Canonical Allele Identifier: PA658665034

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000531246

RCV000598531

ClinVar Variation:

458393

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Val627Ile	CA4704517 NM_000553.6:c.1879G>A