Allele Registry

Canonical Allele Identifier: PA2825764969

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000685812

RCV003144484

ClinVar Variation:

566085

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Pro778Leu	CA49742304 NM_001130984.2:c.2333C>T