Canonical Allele Identifier: PA2828961214
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2862356
ClinVar RCV Id: RCV003699809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372202.1:p.Phe124Ile
CA7083186
NM_001385273.1:c.370T>A