Canonical Allele Identifier: PA2828961162
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1930811
ClinVar RCV Id: RCV002618997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372201.1:p.Arg125Lys
CA389116984
NM_001385272.1:c.374G>A