Canonical Allele Identifier: PA275692
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204101
ClinVar RCV Id: RCV000186307
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Leu150Pro
CA275691
NM_000030.3:c.449T>C