Allele Registry

Canonical Allele Identifier: PA275547

Gene: AGXT HGNC NCBI

ClinVar Allele:

200426

ClinVar RCV:

RCV000186221

RCV000881725

RCV002516973

ClinVar Variation:

204019

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Lys12Arg	CA275546 NM_000030.3:c.35A>G