Canonical Allele Identifier: PA2825920282
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215362
ClinVar RCV Id: RCV000196541 RCV001705134 RCV003126582 RCV004020436 RCV004541267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Glu593Asp
CA320964
NM_001145853.1:c.1779G>C
CA356176830
NM_001145853.1:c.1779G>T