Canonical Allele Identifier: PA2825920225
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439835
ClinVar RCV Id: RCV001950262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala559Ser
CA91796451
NM_001145853.1:c.1675G>T