Allele Registry

Canonical Allele Identifier: PA3057243225

Gene: ANG HGNC NCBI

ClinVar Allele:

33119

ClinVar RCV:

RCV000019706

ClinVar Variation:

18080

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372203.1:p.Ser52Asn	CA258109 NM_001385274.1:c.155G>A