Allele Registry

Canonical Allele Identifier: PA2825765799

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000530924

RCV000664797

RCV000725642

RCV003235177

ClinVar Variation:

285356

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Tyr1502His	CA1707060 NM_001130984.2:c.4504T>C