Allele Registry

Canonical Allele Identifier: PA2825769280

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000007064

ClinVar Variation:

6677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Asp612Tyr	CA253909 NM_001130986.2:c.1834G>T