Allele Registry

Canonical Allele Identifier: PA275618

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186273

RCV004526632

ClinVar Variation:

204067

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Val8Leu	CA275617 NM_000030.3:c.22G>C CA351312678 NM_000030.3:c.22G>T