Allele Registry

Canonical Allele Identifier: PA275749

Gene: AGXT HGNC NCBI

ClinVar Allele:

200566

ClinVar RCV:

RCV000186338

ClinVar Variation:

204132

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gln282His	CA275748 NM_000030.3:c.846G>C CA351318425 NM_000030.3:c.846G>T