Allele Registry

Canonical Allele Identifier: PA2825763472

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 288624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124455.1:p.Arg1424Cys	CA1706966 NM_001130983.2:c.4270C>T