Canonical Allele Identifier: PA275653
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204083
ClinVar RCV Id: RCV000186289 RCV001386863 RCV002271450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ser81Leu
CA275652
NM_000030.3:c.242C>T