Allele Registry

Canonical Allele Identifier: PA2741833822

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003738749

ClinVar Variation:

2912979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Arg1070Pro	CA347217058 NM_001130982.2:c.3209G>C