Canonical Allele Identifier: PA2825765771
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285159
ClinVar RCV Id: RCV000725599 RCV001495704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Gly1461Ser
CA1707026
NM_001130984.2:c.4381G>A