Allele Registry

Canonical Allele Identifier: PA3057243226

Gene: ANG HGNC NCBI

ClinVar RCV:

RCV000019702

ClinVar Variation:

18076

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372203.1:p.Arg55Lys	CA258097 NM_001385274.1:c.164G>A