Canonical Allele Identifier: PA2828961213
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1344517
ClinVar RCV Id: RCV001848613 RCV002034770 RCV002543425 RCV003401757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372202.1:p.Gly123Ala
CA7083184
NM_001385273.1:c.368G>C