Allele Registry

Canonical Allele Identifier: PA645477601

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000007064

ClinVar Variation:

6677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Asp643Tyr	CA253909 NM_001130987.2:c.1927G>T