Canonical Allele Identifier: PA2825523974
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2265845
ClinVar RCV Id: RCV002793464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.His32Gln
CA389113929
NM_001097577.3:c.96C>A
CA389113932
NM_001097577.3:c.96C>G