Allele Registry

Canonical Allele Identifier: PA2825770513

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000374736

RCV000664874

RCV000778917

RCV001329706

RCV001563739

RCV003940011

ClinVar Variation:

285686

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Pro1726Gln	CA1707338 NM_001130986.2:c.5177C>A