Canonical Allele Identifier: PA258105
Gene: ANG HGNC NCBI
ClinVar RCV:
RCV000019704
ClinVar Variation:
18078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Lys64Ile
CA258103
NM_001145.4:c.191A>T