Allele Registry

Canonical Allele Identifier: PA2825763164

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000398537

RCV002518140

ClinVar Variation:

290506

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124455.1:p.Thr1142Met	CA1706576 NM_001130983.2:c.3425C>T