Canonical Allele Identifier: PA275729
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204121
ClinVar RCV Id: RCV000186327 RCV003556224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly216Arg
CA275728
NM_000030.3:c.646G>A
CA351316956
NM_000030.3:c.646G>C