Canonical Allele Identifier: PA2825920453
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2798320
ClinVar RCV Id: RCV003675715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Gly695Asp
CA2839593
NM_001145853.1:c.2084G>A