Canonical Allele Identifier: PA091323
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Met195Arg
CA275712
NM_000030.3:c.584T>G