Allele Registry

Canonical Allele Identifier: PA2825764663

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000300999

RCV000358093

RCV000711546

RCV001084088

RCV001276725

RCV001449924

RCV001820812

ClinVar Variation:

282209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Met452Val	CA1705737 NM_001130984.2:c.1354A>G