Canonical Allele Identifier: PA2825919996
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2293091
ClinVar RCV Id: RCV002873039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Asp425Ala
CA2839292
NM_001145853.1:c.1274A>C