Allele Registry

Canonical Allele Identifier: PA2825758597

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000648014

RCV001829805

RCV003243237

ClinVar Variation:

538642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Glu558Gly	CA1705883 NM_001130981.2:c.1673A>G