Canonical Allele Identifier: PA2826915082
Gene: AGXT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2394426
ClinVar RCV Id: RCV004226013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293102.1:p.Arg427Cys
CA3228918
NM_001306173.2:c.1279C>T