Canonical Allele Identifier: PA2828961158
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1344517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372201.1:p.Gly123Ala
CA7083184
NM_001385272.1:c.368G>C