Canonical Allele Identifier: PA2825920600
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2189687
ClinVar RCV Id: RCV002636865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val779Leu
CA91797067
NM_001145853.1:c.2335G>T
CA356178389
NM_001145853.1:c.2335G>C