Allele Registry

Canonical Allele Identifier: PA2825755943

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000080300

RCV000531528

RCV001273964

RCV001449921

RCV001699034

ClinVar Variation:

94334

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124452.1:p.Ala201Glu	CA147766 NM_001130980.2:c.602C>A