Canonical Allele Identifier: PA2828961210
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 3051906
ClinVar RCV Id: RCV003959800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372202.1:p.Arg119Gln
CA7083178
NM_001385273.1:c.356G>A