Canonical Allele Identifier: PA645395801
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225514
ClinVar RCV Id: RCV000490380 RCV001300481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala616Ser
CA2839519
NM_006005.3:c.1846G>T