Canonical Allele Identifier: PA2828961059
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1381736
ClinVar RCV Id: RCV001922045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372200.1:p.His37Arg
CA7083140
NM_001385271.1:c.110A>G