Canonical Allele Identifier: PA099076
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18082
ClinVar RCV Id: RCV000019708
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Val137Ile
CA258115
NM_001097577.3:c.409G>A