Canonical Allele Identifier: PA2825753967
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_001124451.1:p.Gly457Arg
CA10603801
NM_001130979.2:c.1369G>A
CA347215045
NM_001130979.2:c.1369G>C