Allele Registry

Canonical Allele Identifier: PA275626

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186277

ClinVar Variation:

204071

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Leu26Pro	CA275625 NM_000030.3:c.77T>C