Allele Registry

Canonical Allele Identifier: PA2825758952

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000176653

RCV000553449

RCV001267331

ClinVar Variation:

195961

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Val908Ile	CA242686 NM_001130981.2:c.2722G>A