Canonical Allele Identifier: PA105695
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4524
ClinVar RCV Id: RCV000004782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Lys634Thr
CA253205
NM_001145853.1:c.1901A>C