Allele Registry

Canonical Allele Identifier: PA2825753837

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000329171

RCV001247468

RCV001833378

ClinVar Variation:

287822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Ala346Thr	CA1705596 NM_001130979.2:c.1036G>A