Canonical Allele Identifier: PA2825757665
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538624
ClinVar RCV Id: RCV000647987 RCV001276860 RCV003144428
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Arg1766His
CA1707346
NM_001130980.2:c.5297G>A