Canonical Allele Identifier: PA2580102522
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2064669
ClinVar RCV Id: RCV002953597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Asp255Asn
CA2209229
NM_000030.3:c.763G>A