Canonical Allele Identifier: PA2580119945
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2429383
ClinVar RCV Id: RCV003126320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Trp200Cys
CA370916229
NM_000553.6:c.600G>C
CA370916230
NM_000553.6:c.600G>T