Canonical Allele Identifier: PA099058
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18080
ClinVar RCV Id: RCV000019706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Ser52Asn
CA258109
NM_001097577.3:c.155G>A