Allele Registry

Canonical Allele Identifier: PA2825770760

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000596899

ClinVar Variation:

501582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Cys1958Arg	CA347226529 NM_001130986.2:c.5872T>C