Canonical Allele Identifier: PA915968299
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 807061
ClinVar RCV Id: RCV000995108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Leu18Gln
CA7083128
NM_001145.4:c.53T>A