Canonical Allele Identifier: PA179642
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166584
ClinVar RCV Id: RCV000152671 RCV001719944 RCV002509253 RCV002514938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe413Val
CA179641
NM_006005.3:c.1237T>G