Canonical Allele Identifier: PA180502
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 167850
ClinVar RCV Id: RCV000154149 RCV000355811 RCV000312681 RCV000870981 RCV001174388 RCV002464008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Met306Thr
CA180501
NM_006005.3:c.917T>C