Canonical Allele Identifier: PA091327
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 5640
ClinVar RCV Id: RCV000005994 RCV000420710
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ser205Pro
CA340441
NM_000030.3:c.613T>C