Allele Registry

Canonical Allele Identifier: PA2829468894

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000534201

ClinVar Variation:

471318

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Asp1855Val	CA347223572 NM_003494.4:c.5564A>T