Allele Registry

Canonical Allele Identifier: PA915960931

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000814396

ClinVar Variation:

657724

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Val114Phe	CA370914446 NM_000553.6:c.340G>T