Allele Registry

Canonical Allele Identifier: PA2825693031

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003866056

ClinVar Variation:

3004417

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Gly235Ala	CA347208444 NM_001130455.2:c.704G>C