Canonical Allele Identifier: PA091305
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204115
ClinVar RCV Id: RCV000186321 RCV001222818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Asp201Glu
CA275715
NM_000030.3:c.603C>A
CA351316771
NM_000030.3:c.603C>G