Allele Registry

Canonical Allele Identifier: PA2825747801

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003738749

ClinVar Variation:

2912979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Arg1024Pro	CA347217058 NM_001130976.2:c.3071G>C