Allele Registry

Canonical Allele Identifier: PA2825750981

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000534201

ClinVar Variation:

471318

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124449.1:p.Asp1862Val	CA347223572 NM_001130977.2:c.5585A>T