Allele Registry

Canonical Allele Identifier: PA2825746955

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003866056

ClinVar Variation:

3004417

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Gly234Ala	CA347208444 NM_001130976.2:c.701G>C