Canonical Allele Identifier: PA2825919787
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057020
ClinVar RCV Id: RCV001365933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala307Val
CA2839152
NM_001145853.1:c.920C>T