Canonical Allele Identifier: PA325364
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215411
ClinVar RCV Id: RCV000200779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Gly398Arg
CA325363
NM_006005.3:c.1192G>C