Canonical Allele Identifier: PA658806779
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 497312
ClinVar RCV Id: RCV000596941 RCV000817716 RCV001829634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Arg837Gln
CA1706192
NM_001130987.2:c.2510G>A