Canonical Allele Identifier: PA645425246
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 335297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Asp201Asn
CA10612912
NM_000030.3:c.601G>A