Canonical Allele Identifier: PA091316
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 188985
ClinVar RCV Id: RCV000169364 RCV001386862
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly41Val
CA274216
NM_000030.3:c.122G>T