Allele Registry

Canonical Allele Identifier: PA3057550835

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV005020879

ClinVar Variation:

3586199

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Pro10Thr	CA2208963 NM_000030.3:c.28C>A