Allele Registry

Canonical Allele Identifier: PA2825763935

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000178688

RCV000790680

RCV001384247

RCV001814049

RCV003466987

ClinVar Variation:

94340

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124455.1:p.Asp1859Asn	CA222190 NM_001130983.2:c.5575G>A