Allele Registry

Canonical Allele Identifier: PA3057575699

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV004759723

ClinVar Variation:

3359184

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly41Trp	CA351313173 NM_000030.3:c.121G>T