Allele Registry

Canonical Allele Identifier: PA2829468203

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000306735

RCV000338437

RCV000406757

RCV001055238

RCV001833354

RCV002519192

ClinVar Variation:

285741

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Pro1555Ser	CA1707143 NM_003494.4:c.4663C>T