Canonical Allele Identifier: PA2825920100
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449979
ClinVar RCV Id: RCV000520862 RCV001198043 RCV003126789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ile489Met
CA2839365
NM_001145853.1:c.1467C>G