Canonical Allele Identifier: PA275766
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204139
ClinVar RCV Id: RCV000186346
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Leu316Pro
CA275765
NM_000030.3:c.947T>C