Canonical Allele Identifier: PA275628
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204072
ClinVar RCV Id: RCV000186278 RCV001383728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg36His
CA275627
NM_000030.3:c.107G>A