Canonical Allele Identifier: PA915973468
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 596925
ClinVar RCV Id: RCV000732902 RCV002535298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Gly566Ser
CA1705878
NM_001130982.2:c.1696G>A