Allele Registry

Canonical Allele Identifier: PA2825759996

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000725163

RCV001085921

RCV001276862

RCV003939934

RCV004021072

ClinVar Variation:

281104

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Arg1834Trp	CA1707403 NM_001130981.2:c.5500C>T