Allele Registry

Canonical Allele Identifier: PA2825765783

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000080290

RCV001854416

RCV003460752

ClinVar Variation:

94324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Lys1488Thr	CA222170 NM_001130984.2:c.4463A>C