Allele Registry

Canonical Allele Identifier: PA2825771837

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV001203031

RCV001828630

RCV003145373

ClinVar Variation:

934608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Pro1418His	CA49779936 NM_001130987.2:c.4253C>A