Canonical Allele Identifier: PA2828961165
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1948642
ClinVar RCV Id: RCV002685807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372201.1:p.Val127Ile
CA7083188
NM_001385272.1:c.379G>A