Allele Registry

Canonical Allele Identifier: PA091323

Gene: AGXT HGNC NCBI

ClinVar Allele:

200517

ClinVar RCV:

RCV000186319

RCV001036463

ClinVar Variation:

204113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Met195Arg	CA275712 NM_000030.3:c.584T>G