Canonical Allele Identifier: PA2828961216
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1930811
ClinVar RCV Id: RCV002618997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372202.1:p.Arg125Lys
CA389116984
NM_001385273.1:c.374G>A