Allele Registry

Canonical Allele Identifier: PA645477798

Gene: DYSF HGNC NCBI

ClinVar Allele:

21717

ClinVar RCV:

RCV000007065

ClinVar Variation:

6678

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Glu1773Gly	CA253911 NM_001130987.2:c.5318A>G