Allele Registry

Canonical Allele Identifier: PA916051179

Gene: SLC25A22 HGNC NCBI

ClinVar RCV:

RCV002508755

ClinVar Variation:

1776

HGVS (amino-acid)	Matching Registered Transcripts
NP_078974.1:p.Gly236Trp	CA115174 NM_024698.6:c.706G>T