Allele Registry

Canonical Allele Identifier: PA645477641

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000380360

RCV001246606

RCV001833413

RCV002480056

ClinVar Variation:

290702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Pro952Leu	CA1706296 NM_001130987.2:c.2855C>T