Allele Registry

Canonical Allele Identifier: PA2825754081

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000389310

RCV000726337

RCV001271778

RCV001850449

ClinVar Variation:

289490

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Arg584Cys	CA1705911 NM_001130979.2:c.1750C>T