Allele Registry

Canonical Allele Identifier: PA2825695459

Gene: DYSF HGNC NCBI

ClinVar Allele:

21717

ClinVar RCV:

RCV000007065

ClinVar Variation:

6678

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Glu1735Gly	CA253911 NM_001130455.2:c.5204A>G