Canonical Allele Identifier: PA091326
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 140584
ClinVar RCV Id: RCV000128801 RCV003317095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ser187Phe
CA345702
NM_000030.3:c.560C>T