Canonical Allele Identifier: PA2499233491
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1003124
ClinVar RCV Id: RCV001299641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Asn178Asp
CA370915941
NM_000553.6:c.532A>G