Allele Registry

Canonical Allele Identifier: PA275711

Gene: AGXT HGNC NCBI

ClinVar Allele:

200516

ClinVar RCV:

RCV000186318

ClinVar Variation:

204112

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Met195Leu	CA275710 NM_000030.3:c.583A>C CA351316606 NM_000030.3:c.583A>T