Allele Registry

Canonical Allele Identifier: PA2825756074

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000080333

RCV000696449

RCV001831823

RCV003330426

ClinVar Variation:

94365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124452.1:p.Val317Glu	CA222220 NM_001130980.2:c.950T>A