Allele Registry

Canonical Allele Identifier: PA658800280

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000633207

RCV003153773

ClinVar Variation:

528123

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ala1260Thr	CA4705173 NM_000553.6:c.3778G>A