Allele Registry

Canonical Allele Identifier: PA2825756870

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003738749

ClinVar Variation:

2912979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124452.1:p.Arg1055Pro	CA347217058 NM_001130980.2:c.3164G>C