Allele Registry

Canonical Allele Identifier: PA2825765236

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000313635

RCV000666376

RCV000701610

RCV002494839

ClinVar Variation:

284003

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Pro1007Leu	CA1706432 NM_001130984.2:c.3020C>T