Canonical Allele Identifier: PA2825920604
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1678045
ClinVar RCV Id: RCV002224636
ClinVar Variation Id: 2166853
ClinVar RCV Id: RCV003080291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Met781Ile
CA2839689
NM_001145853.1:c.2343G>A
CA356178402
NM_001145853.1:c.2343G>C
CA356178403
NM_001145853.1:c.2343G>T