Canonical Allele Identifier: PA258096
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18075
ClinVar RCV Id: RCV000019701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Lys41Glu
CA258094
NM_001145.4:c.121A>G