Canonical Allele Identifier: PA105482
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 516852
ClinVar RCV Id: RCV000730495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala58Val
CA2838811
NM_001145853.1:c.173C>T