Canonical Allele Identifier: PA916010337
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 805751
ClinVar RCV Id: RCV000993555 RCV002509586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Leu388Val
CA356174373
NM_006005.3:c.1162C>G