Allele Registry

Canonical Allele Identifier: PA2825748716

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000534201

ClinVar Variation:

471318

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Asp1841Val	CA347223572 NM_001130976.2:c.5522A>T