Allele Registry

Canonical Allele Identifier: PA2825766659

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003866056

ClinVar Variation:

3004417

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Gly266Ala	CA347208444 NM_001130985.2:c.797G>C