Allele Registry

Canonical Allele Identifier: PA2825760046

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000265900

RCV001859602

RCV003401247

ClinVar Variation:

284471

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Val1878Met	CA10604806 NM_001130981.2:c.5632G>A