Allele Registry

Canonical Allele Identifier: PA645477758

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000306735

RCV000338437

RCV000406757

RCV001055238

RCV001833354

RCV002519192

ClinVar Variation:

285741

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Pro1594Ser	CA1707143 NM_001130987.2:c.4780C>T