Canonical Allele Identifier: PA275622
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204069
ClinVar RCV Id: RCV000186275 RCV001553704 RCV001857587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Pro11Arg
CA275621
NM_000030.3:c.32C>G