Canonical Allele Identifier: PA2825920121
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1973615
ClinVar RCV Id: RCV002765362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Asn500Ser
CA356175199
NM_001145853.1:c.1499A>G
CA2580071772
NM_001145853.1:c.1499_1500delinsGT