Canonical Allele Identifier: PA1139669437
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 835818
ClinVar RCV Id: RCV001036793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Asn199Ser
CA370916213
NM_000553.6:c.596A>G