Canonical Allele Identifier: PA099018
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18078
ClinVar RCV Id: RCV000019704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Lys64Ile
CA258103
NM_001097577.3:c.191A>T