Allele Registry

Canonical Allele Identifier: PA2829467262

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003738749

ClinVar Variation:

2912979

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1038Pro	CA347217058 NM_003494.4:c.3113G>C