Canonical Allele Identifier: PA091312
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 40166
ClinVar RCV Id: RCV000032681 RCV000432954 RCV000589490 RCV003407388
ClinVar Variation Id: 2710435
ClinVar RCV Id: RCV003552420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly170Arg
CA343785
NM_000030.3:c.508G>A
CA68178405
NM_000030.3:c.508G>C