Allele Registry

Canonical Allele Identifier: PA2825692883

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000301411

RCV001082288

RCV001833344

RCV003091891

ClinVar Variation:

285148

2166693

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Gly156Arg	CA1705380 NM_001130455.2:c.466G>A CA49758528 NM_001130455.2:c.466G>C