Canonical Allele Identifier: PA185323
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179874
ClinVar RCV Id: RCV000156674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Leu549Val
CA185322
NM_006005.3:c.1645C>G