Allele Registry

Canonical Allele Identifier: PA658674709

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000552425

RCV000595695

RCV001274843

RCV001507565

RCV003960357

ClinVar Variation:

471308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Val1543Ile	CA1707094 NM_001130987.2:c.4627G>A