Canonical Allele Identifier: PA2741809334
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2664132
ClinVar RCV Id: RCV003445278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Tyr260Cys
CA351318292
NM_000030.3:c.779A>G