Canonical Allele Identifier: PA2825523980
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2212376
ClinVar RCV Id: RCV002677396 RCV003574981
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Gln43His
CA7083141
NM_001097577.3:c.129G>C
CA389114220
NM_001097577.3:c.129G>T