Canonical Allele Identifier: PA275690
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204100
ClinVar RCV Id: RCV000186306
ClinVar Variation Id: 553340
ClinVar RCV Id: RCV000668762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Glu141Asp
CA275689
NM_000030.3:c.423G>T
CA351314700
NM_000030.3:c.423G>C