Allele Registry

Canonical Allele Identifier: PA2825695683

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000534201

ClinVar Variation:

471318

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Asp1856Val	CA347223572 NM_001130455.2:c.5567A>T