Canonical Allele Identifier: PA258099
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18076
ClinVar RCV Id: RCV000019702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Arg55Lys
CA258097
NM_001145.4:c.164G>A