Canonical Allele Identifier: PA091310
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 5650
ClinVar RCV Id: RCV000006004 RCV001851686 RCV002265548
ClinVar Variation Id: 552979
ClinVar RCV Id: RCV000668336 RCV002530741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly156Arg
CA340448
NM_000030.3:c.466G>A
CA68178380
NM_000030.3:c.466G>C