Canonical Allele Identifier: PA091313
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 189047
ClinVar RCV Id: RCV000169439 RCV000816747
ClinVar Variation Id: 2577088
ClinVar RCV Id: RCV003324165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly190Arg
CA274318
NM_000030.3:c.568G>A
CA351316577
NM_000030.3:c.568G>C