Canonical Allele Identifier: PA091301
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 5648
ClinVar RCV Id: RCV000006002 RCV001385647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg233His
CA253545
NM_000030.3:c.698G>A