Allele Registry

Canonical Allele Identifier: PA3057550840

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV005020880

ClinVar Variation:

3586201

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly42Arg	CA2208982 NM_000030.3:c.124G>A CA351313180 NM_000030.3:c.124G>C