Allele Registry

Canonical Allele Identifier: PA891854619

Gene: WRN HGNC NCBI

ClinVar Variation Id: 581431

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ser1128Arg	CA370924244 NM_000553.6:c.3382A>C CA370925125 NM_000553.6:c.3384T>A CA370925127 NM_000553.6:c.3384T>G