Canonical Allele Identifier: PA274059
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 188866
ClinVar RCV Id: RCV000169219 RCV001850392
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Leu101Pro
CA274058
NM_000030.3:c.302T>C