Canonical Allele Identifier: PA275790
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204150
ClinVar RCV Id: RCV000186357 RCV002516975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Leu384Pro
CA275789
NM_000030.3:c.1151T>C