Canonical Allele Identifier: PA645485533
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 312774
ClinVar RCV Id: RCV000516549 RCV000877109 RCV000986163 RCV003940211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Lys84Glu
CA7083167
NM_001145.4:c.250A>G