Canonical Allele Identifier: PA091300
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 5647
ClinVar RCV Id: RCV000006001 RCV001070457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg233Cys
CA340446
NM_000030.3:c.697C>T