Allele Registry

Canonical Allele Identifier: PA2825747916

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000284503

RCV000648010

ClinVar Variation:

282705

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Val1105Met	CA1706555 NM_001130976.2:c.3313G>A