Canonical Allele Identifier: PA091328
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 188979
ClinVar RCV Id: RCV000169358 RCV001386996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ser218Leu
CA274210
NM_000030.3:c.653C>T