Canonical Allele Identifier: PA2573159784
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1511903
ClinVar RCV Id: RCV002020644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Trp251Arg
CA2209226
NM_000030.3:c.751T>C
CA351318219
NM_000030.3:c.751T>A