Canonical Allele Identifier: PA2825695886
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 501582
ClinVar RCV Id: RCV000596899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Cys1972Arg
CA347226529
NM_001130455.2:c.5914T>C