Canonical Allele Identifier: PA2825694722
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 852049
ClinVar RCV Id: RCV001056589 RCV001272841 RCV003145310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Arg1298Gly
CA1706803
NM_001130455.2:c.3892A>G