Canonical Allele Identifier: PA275616
Gene: AGXT HGNC NCBI
ClinVar Allele:
200418
ClinVar RCV:
RCV000186272
ClinVar Variation:
204066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Met1Ile