Canonical Allele Identifier: PA2826135569
Gene: ACE HGNC NCBI

Linked Data

ClinVar Variation Id: 1577402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171528.1:p.Arg675Trp
CA8700680
NM_001178057.2:c.2023C>T