Canonical Allele Identifier: PA2828961186
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1730747
ClinVar RCV Id: RCV002451756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372202.1:p.Tyr38Cys
CA389114097
NM_001385273.1:c.113A>G