Canonical Allele Identifier: PA275738
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204127
ClinVar RCV Id: RCV000186333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.His261Gln
CA275737
NM_000030.3:c.783T>A
CA351318300
NM_000030.3:c.783T>G