Canonical Allele Identifier: PA275742
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204129
ClinVar RCV Id: RCV000186335 RCV001852426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Glu274Asp
CA275741
NM_000030.3:c.822G>C
CA351318383
NM_000030.3:c.822G>T