Canonical Allele Identifier: PA2825760456
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 286920
ClinVar RCV Id: RCV000342489 RCV001273965 RCV000793369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Gly210Arg
CA1705397
NM_001130982.2:c.628G>A
CA347207062
NM_001130982.2:c.628G>C