Allele Registry

Canonical Allele Identifier: PA275744

Gene: AGXT HGNC NCBI

ClinVar Variation Id: 204130

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ser275Arg	CA275743 NM_000030.3:c.823A>C CA351318388 NM_000030.3:c.825C>A CA351318389 NM_000030.3:c.825C>G