Canonical Allele Identifier: PA2825920101
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 505052
ClinVar RCV Id: RCV000614284 RCV003126843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Thr490Ala
CA356175084
NM_001145853.1:c.1468A>G