Canonical Allele Identifier: PA091309
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 189021
ClinVar RCV Id: RCV000169408 RCV001236818 RCV001814082
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly116Arg
CA274270
NM_000030.3:c.346G>A
CA351313961
NM_000030.3:c.346G>C