Canonical Allele Identifier: PA2825766879
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281067
ClinVar RCV Id: RCV000379326 RCV001244501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Gly458Arg
CA10603801
NM_001130985.2:c.1372G>A
CA347215045
NM_001130985.2:c.1372G>C