Allele Registry

Canonical Allele Identifier: PA645477628

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000080253

RCV000326704

RCV000381491

RCV000528879

RCV001274456

RCV001795100

ClinVar Variation:

94289

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Ile852Val	CA147734 NM_001130987.2:c.2554A>G