Canonical Allele Identifier: PA645477688
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284252
ClinVar RCV Id: RCV000316493 RCV001855139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Leu1288Arg
CA10604735
NM_001130987.2:c.3863T>G