Canonical Allele Identifier: PA275699
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204105
ClinVar RCV Id: RCV000186311 RCV000662317 RCV001069631 RCV003226241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly161Ser
CA275698
NM_000030.3:c.481G>A