Canonical Allele Identifier: PA658800127
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 528183
ClinVar RCV Id: RCV000633267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Tyr224Asn
CA370916924
NM_000553.6:c.670T>A