Canonical Allele Identifier: PA2825694441
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282705
ClinVar RCV Id: RCV000284503 RCV000648010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Val1120Met
CA1706555
NM_001130455.2:c.3358G>A