Allele Registry

Canonical Allele Identifier: PA645477616

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000300931

RCV000405461

RCV000726455

RCV001082501

RCV001271788

RCV003910038

ClinVar Variation:

290257

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.His753Asn	CA1706110 NM_001130987.2:c.2257C>A