Allele Registry

Canonical Allele Identifier: PA156016

Gene: WRN HGNC NCBI

ClinVar Variation Id: 130757

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Met387Ile	CA156014 NM_000553.6:c.1161G>A CA370921027 NM_000553.6:c.1161G>C CA370921030 NM_000553.6:c.1161G>T