Canonical Allele Identifier: PA2828961056
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2265845
ClinVar RCV Id: RCV002793464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372200.1:p.His32Gln
CA389113929
NM_001385271.1:c.96C>A
CA389113932
NM_001385271.1:c.96C>G