Allele Registry

Canonical Allele Identifier: PA2580119930

Gene: WRN HGNC NCBI

ClinVar Variation Id: 2049584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ser198Arg	CA370916195 NM_000553.6:c.592A>C CA370916202 NM_000553.6:c.594C>A CA370916203 NM_000553.6:c.594C>G