Canonical Allele Identifier: PA2825920456
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406273
ClinVar RCV Id: RCV001935385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg697Ser
CA2839595
NM_001145853.1:c.2091G>C
CA356177684
NM_001145853.1:c.2091G>T