Allele Registry

Canonical Allele Identifier: PA3057576119

Gene: ANG HGNC NCBI

ClinVar Allele:

33113

ClinVar RCV:

RCV000019700

RCV000517735

RCV001642231

RCV003934843

ClinVar Variation:

18074

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372203.1:p.Lys41Ile	CA258091 NM_001385274.1:c.122A>T