Canonical Allele Identifier: PA179628
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166568
ClinVar RCV Id: RCV000152662 RCV002509039
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala43Val
CA179627
NM_006005.3:c.128C>T