Allele Registry

Canonical Allele Identifier: PA2825760089

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000317613

RCV000754725

RCV002521880

ClinVar Variation:

282408

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Tyr1915His	CA1707485 NM_001130981.2:c.5743T>C