Canonical Allele Identifier: PA2580317442
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2164677
ClinVar RCV Id: RCV003088156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ile561Leu
CA91796459
NM_006005.3:c.1681A>C