Canonical Allele Identifier: PA2825793754
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2322998
ClinVar RCV Id: RCV002920418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Ala120Asp
CA389116775
NM_001145.4:c.359C>A