Allele Registry

Canonical Allele Identifier: PA2826915057

Gene: AGXT2 HGNC NCBI

ClinVar RCV:

RCV000490599

ClinVar Variation:

427577

HGVS (amino-acid)	Matching Registered Transcripts
NP_001293102.1:p.Val140Ile	CA3229361 NM_001306173.2:c.418G>A