Allele Registry

Canonical Allele Identifier: PA275685

Gene: AGXT HGNC NCBI

ClinVar Allele:

200483

ClinVar RCV:

RCV000186304

ClinVar Variation:

204098

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.His124Pro	CA275684 NM_000030.3:c.371A>C