Canonical Allele Identifier: PA1139668682
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 957713
ClinVar RCV Id: RCV001230740 RCV001833997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Leu24Ile
CA2208974
NM_000030.3:c.70C>A