Canonical Allele Identifier: PA2825920243
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2080395
ClinVar RCV Id: RCV003001894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Phe568Ser
CA91796476
NM_001145853.1:c.1703T>C