Canonical Allele Identifier: PA645395860
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229641
ClinVar RCV Id: RCV000218719 RCV001393083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ser790Leu
CA2839705
NM_006005.3:c.2369C>T