Allele Registry

Canonical Allele Identifier: PA2580122248

Gene: WRN HGNC NCBI

ClinVar Variation Id: 1720388

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Phe1431Leu	CA370911938 NM_000553.6:c.4291T>C CA370911943 NM_000553.6:c.4293T>A CA370911944 NM_000553.6:c.4293T>G