Canonical Allele Identifier: PA2825793752
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 3051906
ClinVar RCV Id: RCV003959800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Arg119Gln
CA7083178
NM_001145.4:c.356G>A