Canonical Allele Identifier: PA2828961208
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2636742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372202.1:p.Arg119Leu
CA7083179
NM_001385273.1:c.356G>T