Canonical Allele Identifier: PA099001
Gene: ANG HGNC NCBI
ClinVar RCV:
RCV000019701
ClinVar Variation:
18075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Lys41Glu
CA258094
NM_001097577.3:c.121A>G