Canonical Allele Identifier: PA2741809333
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2664131
ClinVar RCV Id: RCV003445277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg258Ser
CA2209231
NM_000030.3:c.774G>T
CA351318270
NM_000030.3:c.774G>C