Canonical Allele Identifier: PA2825524011
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 225053
ClinVar RCV Id: RCV000210667
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Pro136Ser
CA358172
NM_001097577.3:c.406C>T