Allele Registry

Canonical Allele Identifier: PA2825751695

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000297254

RCV000392981

RCV000705827

RCV001828331

ClinVar Variation:

336950

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124450.1:p.Ala425Val	CA1705708 NM_001130978.2:c.1274C>T