Allele Registry

Canonical Allele Identifier: PA2825758675

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000007064

ClinVar Variation:

6677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Asp642Tyr	CA253909 NM_001130981.2:c.1924G>T