Canonical Allele Identifier: PA1139668765
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 961691
ClinVar RCV Id: RCV001235424 RCV002484288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly120Arg
CA2209058
NM_000030.3:c.358G>A
CA351314029
NM_000030.3:c.358G>C