Allele Registry

Canonical Allele Identifier: PA2825770640

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000534201

ClinVar Variation:

471318

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Asp1842Val	CA347223572 NM_001130986.2:c.5525A>T