Allele Registry

Canonical Allele Identifier: PA150819

Gene: SLC25A22 HGNC NCBI

ClinVar RCV:

RCV002508764

ClinVar Variation:

120308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177990.1:p.Gly110Arg	CA150818 NM_001191061.2:c.328G>C