Allele Registry

Canonical Allele Identifier: PA2825767110

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000251223

RCV000513999

RCV001081560

RCV001828138

RCV002519917

ClinVar Variation:

259069

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Leu703Val	CA1706042 NM_001130985.2:c.2107C>G