Allele Registry

Canonical Allele Identifier: PA658806698

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000592160

RCV000807941

RCV001276724

ClinVar Variation:

500618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Ser455Thr	CA1705707 NM_001130987.2:c.1364G>C