Allele Registry

Canonical Allele Identifier: PA2825695518

Gene: DYSF HGNC NCBI

ClinVar Allele:

266861

ClinVar RCV:

RCV000266653

RCV000725114

RCV000757894

RCV001141002

RCV001810440

RCV003463743

ClinVar Variation:

282624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Arg1769Gln	CA1707357 NM_001130455.2:c.5306G>A