Allele Registry

Canonical Allele Identifier: PA2825747661

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000380360

RCV001246606

RCV001833413

RCV002480056

ClinVar Variation:

290702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Pro920Leu	CA1706296 NM_001130976.2:c.2759C>T