Canonical Allele Identifier: PA645395789
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229639
ClinVar RCV Id: RCV000218792 RCV002485409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala569Thr
CA10576639
NM_006005.3:c.1705G>A