Canonical Allele Identifier: PA091299
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204093
ClinVar RCV Id: RCV000186299 RCV003556222
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ala112Asp
CA275673
NM_000030.3:c.335C>A