Allele Registry

Canonical Allele Identifier: PA915974182

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000658870

RCV001140901

RCV001196059

ClinVar Variation:

501040

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Val1435Ile	CA1706946 NM_001130982.2:c.4303G>A