Canonical Allele Identifier: PA2741809269
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2681163
ClinVar RCV Id: RCV003468688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly116Trp
CA351313963
NM_000030.3:c.346G>T