Allele Registry

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Canonical Allele Identifier: PA2829468862

Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1980346

ClinVar RCV Id: RCV002780231

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Gly1832Arg	CA347222985 NM_003494.4:c.5494G>A CA347222987 NM_003494.4:c.5494G>C