Canonical Allele Identifier: PA645395727
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229648
ClinVar RCV Id: RCV000220517 RCV001325067 RCV002485411 RCV002509310 RCV004020642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe331Ile
CA2839183
NM_006005.3:c.991T>A