Allele Registry

Canonical Allele Identifier: PA658665206

Gene: WRN HGNC NCBI

ClinVar Variation Id: 458480

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Phe1411Leu	CA370911665 NM_000553.6:c.4231T>C CA370911676 NM_000553.6:c.4233T>A CA370911677 NM_000553.6:c.4233T>G