Allele Registry

Canonical Allele Identifier: PA3057243228

Gene: ANG HGNC NCBI

ClinVar RCV:

RCV000019704

ClinVar Variation:

18078

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372203.1:p.Lys64Ile	CA258103 NM_001385274.1:c.191A>T