Allele Registry

Canonical Allele Identifier: PA3057243229

Gene: ANG HGNC NCBI

ClinVar RCV:

RCV000019708

ClinVar Variation:

18082

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372203.1:p.Val137Ile	CA258115 NM_001385274.1:c.409G>A