Allele Registry

Canonical Allele Identifier: PA915974222

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000080287

RCV000177998

RCV000536105

RCV003460751

RCV003993797

ClinVar Variation:

94321

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Gly1450Asp	CA222164 NM_001130982.2:c.4349G>A