Allele Registry

Canonical Allele Identifier: PA343787

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000032682

RCV000247828

RCV001519689

ClinVar Variation:

39486

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ile340Met	CA343786 NM_000030.3:c.1020A>G