Canonical Allele Identifier: PA658800267
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 528180
ClinVar RCV Id: RCV000633264
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Met1130Thr
CA4705053
NM_000553.6:c.3389T>C