Allele Registry

Canonical Allele Identifier: PA275614

Gene: AGXT HGNC NCBI

ClinVar Allele:

200416

ClinVar RCV:

RCV000186271

RCV001061218

ClinVar Variation:

204065

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Met1Thr