Allele Registry

Canonical Allele Identifier: PA2825693627

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000007064

ClinVar Variation:

6677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Asp626Tyr	CA253909 NM_001130455.2:c.1876G>T