Allele Registry

Canonical Allele Identifier: PA2825767507

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003738749

ClinVar Variation:

2912979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Arg1056Pro	CA347217058 NM_001130985.2:c.3167G>C