Allele Registry

Canonical Allele Identifier: PA2825753558

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000596973

RCV000725459

RCV003736685

ClinVar Variation:

284469

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Val69Gly	CA10604804 NM_001130979.2:c.206T>G