Canonical Allele Identifier: PA352233
Gene: AGXT HGNC NCBI
ClinVar RCV:
RCV003445720
ClinVar Variation:
242577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Val102_Gly103insValLeuVal
CA352232
NM_000030.3:c.299_307dup