Canonical Allele Identifier: PA2828961193
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1428243
ClinVar RCV Id: RCV001936212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372202.1:p.Arg57Gln
CA7083151
NM_001385273.1:c.170G>A