Canonical Allele Identifier: PA105624
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4510
ClinVar RCV Id: RCV000004768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Gly695Val
CA253186
NM_001145853.1:c.2084G>T