Canonical Allele Identifier: PA2825919683
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2915997
ClinVar RCV Id: RCV003740245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Lys221Arg
CA2838990
NM_001145853.1:c.662A>G