Allele Registry

Canonical Allele Identifier: PA162718

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122279

RCV000344080

RCV000857870

ClinVar Variation:

135423

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Lys32Arg	CA162716 NM_000553.6:c.95A>G