Canonical Allele Identifier: PA321768
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215414
ClinVar RCV Id: RCV000197313 RCV000300930 RCV000339404 RCV003147402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg818His
CA321767
NM_006005.3:c.2453G>A