Canonical Allele Identifier: PA2573170646
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1494873
ClinVar RCV Id: RCV001989634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Arg1427Lys
CA4705314
NM_000553.6:c.4280G>A