Canonical Allele Identifier: PA1139686750
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 882865
ClinVar RCV Id: RCV001112906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Val13Ala
CA7083122
NM_001145.4:c.38T>C