Allele Registry

Canonical Allele Identifier: PA645437152

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000227669

RCV000858340

RCV003919923

ClinVar Variation:

238128

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Thr573Ala	CA4704456 NM_000553.6:c.1717A>G