Canonical Allele Identifier: PA275641
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204078
ClinVar RCV Id: RCV000186284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Glu59Lys
CA275640
NM_000030.3:c.175G>A