Canonical Allele Identifier: PA2825693667
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 195598
ClinVar RCV Id: RCV000292466 RCV000328757 RCV000487642 RCV001085988 RCV001563948 RCV001563950 RCV001563949 RCV003416078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Lys657Glu
CA242074
NM_001130455.2:c.1969A>G