Allele Registry

Canonical Allele Identifier: PA3057575685

Gene: ANG HGNC NCBI

ClinVar Allele:

33118

ClinVar RCV:

RCV000019705

RCV000335176

RCV001659725

RCV003974847

ClinVar Variation:

18079

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372203.1:p.Ile70Val	CA258106 NM_001385274.1:c.208A>G