Canonical Allele Identifier: PA658757560
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 493139
ClinVar RCV Id: RCV000585002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Lys78Glu
CA7083161
NM_001145.4:c.232A>G