Allele Registry

Canonical Allele Identifier: PA658800212

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV001163334

RCV001572660

ClinVar Variation:

528204

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Val780Ile	CA4704723 NM_000553.6:c.2338G>A