Allele Registry

Canonical Allele Identifier: PA2829466501

Gene: DYSF HGNC NCBI

ClinVar Allele:

535273

ClinVar RCV:

RCV000656079

RCV001089586

RCV001220606

ClinVar Variation:

545009

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Leu556Pro	CA1705913 NM_003494.4:c.1667T>C