Allele Registry

Canonical Allele Identifier: PA2826171458

Gene: SLC25A22 HGNC NCBI

ClinVar RCV:

RCV002508755

ClinVar Variation:

1776

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177989.1:p.Gly236Trp	CA115174 NM_001191060.2:c.706G>T