Canonical Allele Identifier: PA275680
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204096
ClinVar RCV Id: RCV000186302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg118His
CA275679
NM_000030.3:c.353G>A