Allele Registry

Canonical Allele Identifier: PA2825763395

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000266054

RCV002518100

ClinVar Variation:

289774

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124455.1:p.Val1359Met	CA1706898 NM_001130983.2:c.4075G>A