Allele Registry

Canonical Allele Identifier: PA1139682526

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 959188

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Met658Ile	CA347218667 NM_001130982.2:c.1974G>A CA347218668 NM_001130982.2:c.1974G>C CA347218669 NM_001130982.2:c.1974G>T