Allele Registry

Canonical Allele Identifier: PA2825749373

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000264809

RCV001241483

RCV001828209

RCV002521928

ClinVar Variation:

284934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124449.1:p.Gly378Glu	CA1705655 NM_001130977.2:c.1133G>A