Canonical Allele Identifier: PA091325
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204103
ClinVar RCV Id: RCV000186309 RCV001233993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ser158Leu
CA275694
NM_000030.3:c.473C>T