Allele Registry

Canonical Allele Identifier: PA915973601

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000300931

RCV000405461

RCV000726455

RCV001082501

RCV001271788

RCV003910038

ClinVar Variation:

290257

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.His767Asn	CA1706110 NM_001130982.2:c.2299C>A