Canonical Allele Identifier: PA891863501
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 591231
ClinVar RCV Id: RCV000722408 RCV003126921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe538Ser
CA356176267
NM_006005.3:c.1613T>C