Canonical Allele Identifier: PA2825919422
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393384
ClinVar RCV Id: RCV000445526 RCV002488989 RCV002509070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala58Thr
CA16609249
NM_001145853.1:c.172G>A