Canonical Allele Identifier: PA2825768878
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 259085
ClinVar RCV Id: RCV000249294 RCV000532146 RCV000733997 RCV001833275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Val227Met
CA1705456
NM_001130986.2:c.679G>A