Canonical Allele Identifier: PA258117
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18082
ClinVar RCV Id: RCV000019708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Val137Ile
CA258115
NM_001145.4:c.409G>A