Canonical Allele Identifier: PA2825524004
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 312776
ClinVar RCV Id: RCV000284382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Ala122Val
CA7083182
NM_001097577.3:c.365C>T