Allele Registry

Canonical Allele Identifier: PA645437396

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000232120

RCV001356218

RCV003919924

ClinVar Variation:

238150

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Lys1087Glu	CA4704995 NM_000553.6:c.3259A>G