Allele Registry

Canonical Allele Identifier: PA2741809275

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV003445268

ClinVar Variation:

2664122

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Arg118Pro	CA2209057 NM_000030.3:c.353G>C