Canonical Allele Identifier: PA275685
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204098
ClinVar RCV Id: RCV000186304
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.His124Pro
CA275684
NM_000030.3:c.371A>C