Canonical Allele Identifier: PA179632
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166570
ClinVar RCV Id: RCV000152664 RCV000664085 RCV000727284 RCV002509041 RCV002516064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.His109Tyr
CA179631
NM_006005.3:c.325C>T