Canonical Allele Identifier: PA2825793779
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1948642
ClinVar RCV Id: RCV002685807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Val127Ile
CA7083188
NM_001145.4:c.379G>A