Canonical Allele Identifier: PA275660
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204087
ClinVar RCV Id: RCV000186293 RCV001352204
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Glu95Lys
CA275659
NM_000030.3:c.283G>A