Canonical Allele Identifier: PA273898
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 188738
ClinVar RCV Id: RCV000169046 RCV001066143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly161Cys
CA273897
NM_000030.3:c.481G>T