Canonical Allele Identifier: PA2825920271
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949627
ClinVar RCV Id: RCV002676359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala586Val
CA356176763
NM_001145853.1:c.1757C>T