Allele Registry

Canonical Allele Identifier: PA2825763028

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003738749

ClinVar Variation:

2912979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124455.1:p.Arg1039Pro	CA347217058 NM_001130983.2:c.3116G>C