Allele Registry

Canonical Allele Identifier: PA110877

Gene: DYSF HGNC NCBI

ClinVar Allele:

21717

ClinVar RCV:

RCV000007065

ClinVar Variation:

6678

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Glu1734Gly	CA253911 NM_003494.4:c.5201A>G