Canonical Allele Identifier: PA2825920050
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229636
ClinVar RCV Id: RCV000217826 RCV003126610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Thr461Ile
CA10576638
NM_001145853.1:c.1382C>T