Canonical Allele Identifier: PA091308
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Cys253Arg
CA275736
NM_000030.3:c.757T>C