Canonical Allele Identifier: PA275840
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204189
ClinVar RCV Id: RCV000186396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ala186_Ser187delinsAspArg
CA275836
NM_000030.3:c.557_562delinsATCGGT