Canonical Allele Identifier: PA1139671521
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 944095
ClinVar RCV Id: RCV001214421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Cys1041Tyr
CA370922549
NM_000553.6:c.3122G>A