Canonical Allele Identifier: PA275722
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204118
ClinVar RCV Id: RCV000186324 RCV001857589 RCV002307437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ser205Leu
CA275721
NM_000030.3:c.614C>T