Allele Registry

Canonical Allele Identifier: PA2825754070

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000648014

RCV001829805

RCV003243237

ClinVar Variation:

538642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Glu572Gly	CA1705883 NM_001130979.2:c.1715A>G