Canonical Allele Identifier: PA275711
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204112
ClinVar RCV Id: RCV000186318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Met195Leu
CA275710
NM_000030.3:c.583A>C
CA351316606
NM_000030.3:c.583A>T