Canonical Allele Identifier: PA105515
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215389
ClinVar RCV Id: RCV000488089 RCV000603890 RCV001153150 RCV001153151 RCV001174421 RCV000765780 RCV001375054 RCV001640297 RCV004530181 RCV004020439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg457Ser
CA320009
NM_001145853.1:c.1371G>T
CA356174774
NM_001145853.1:c.1371G>C