Allele Registry

Canonical Allele Identifier: PA2825769109

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000297254

RCV000392981

RCV000705827

RCV001828331

ClinVar Variation:

336950

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Ala426Val	CA1705708 NM_001130986.2:c.1277C>T