Canonical Allele Identifier: PA2828961089
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2636742
ClinVar RCV Id: RCV003422511 RCV003553930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372200.1:p.Arg119Leu
CA7083179
NM_001385271.1:c.356G>T