Allele Registry

Canonical Allele Identifier: PA275702

Gene: AGXT HGNC NCBI

ClinVar Allele:

200504

ClinVar RCV:

RCV000186313

ClinVar Variation:

204107

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Leu166Pro	CA275701 NM_000030.3:c.497T>C