Canonical Allele Identifier: PA645477795
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282885
ClinVar RCV Id: RCV000689268 RCV000711566 RCV001274852 RCV003278732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Arg1759His
CA1707309
NM_001130987.2:c.5276G>A