Canonical Allele Identifier: PA3057243229
Gene: ANG HGNC NCBI
ClinVar Allele:
33121
ClinVar RCV:
RCV000019708
ClinVar Variation:
18082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372203.1:p.Val137Ile
CA258115
NM_001385274.1:c.409G>A