Canonical Allele Identifier: PA258102
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18077
ClinVar RCV Id: RCV000019703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Cys63Trp
CA258100
NM_001145.4:c.189C>G