Canonical Allele Identifier: PA275606
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204060
ClinVar RCV Id: RCV000186266 RCV001753585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg381Lys
CA275605
NM_000030.3:c.1142G>A