Allele Registry

Canonical Allele Identifier: PA2829468697

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000266653

RCV000725114

RCV000757894

RCV001141002

RCV001810440

RCV003463743

ClinVar Variation:

282624

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1768Gln	CA1707357 NM_003494.4:c.5303G>A