Canonical Allele Identifier: PA1139668699
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 898216
ClinVar RCV Id: RCV001141969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Asp58Glu
CA68173735
NM_000030.3:c.174C>A
CA351313362
NM_000030.3:c.174C>G