Allele Registry

Canonical Allele Identifier: PA2825754979

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 286443

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Thr1396Met	CA1706904 NM_001130979.2:c.4187C>T