Canonical Allele Identifier: PA275749
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204132
ClinVar RCV Id: RCV000186338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gln282His
CA275748
NM_000030.3:c.846G>C
CA351318425
NM_000030.3:c.846G>T