Allele Registry

Canonical Allele Identifier: PA2825768420

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000534201

ClinVar Variation:

471318

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Asp1873Val	CA347223572 NM_001130985.2:c.5618A>T