Canonical Allele Identifier: PA2825763829
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538624
ClinVar RCV Id: RCV000647987 RCV001276860 RCV003144428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Arg1771His
CA1707346
NM_001130983.2:c.5312G>A