Canonical Allele Identifier: PA275545
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204018
ClinVar RCV Id: RCV000186220 RCV000884267 RCV003416113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Pro11His
CA275544
NM_000030.3:c.32C>A