Canonical Allele Identifier: PA275672
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204092
ClinVar RCV Id: RCV000186298 RCV002305454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg111Gln
CA275671
NM_000030.3:c.332G>A