Canonical Allele Identifier: PA179640
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166583
ClinVar RCV Id: RCV000152670 RCV001308356 RCV002505159 RCV002509252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.His407Tyr
CA179639
NM_006005.3:c.1219C>T