Canonical Allele Identifier: PA2825920363
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166599
ClinVar RCV Id: RCV000152683 RCV001857526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Thr641Lys
CA179659
NM_001145853.1:c.1922C>A