Canonical Allele Identifier: PA275639
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204077
ClinVar RCV Id: RCV000186283 RCV003230441 RCV003229816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ile56Asn
CA275638
NM_000030.3:c.167T>A