Allele Registry

Canonical Allele Identifier: PA3057550844

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV004691053

ClinVar Variation:

3336473

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly82Ala	CA351313535 NM_000030.3:c.245G>C