Allele Registry

Canonical Allele Identifier: PA258099

Gene: ANG HGNC NCBI

ClinVar Allele:

33115

ClinVar RCV:

RCV000019702

ClinVar Variation:

18076

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136.1:p.Arg55Lys	CA258097 NM_001145.4:c.164G>A