Allele Registry

Canonical Allele Identifier: PA258096

Gene: ANG HGNC NCBI

ClinVar Allele:

33114

ClinVar RCV:

RCV000019701

ClinVar Variation:

18075

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136.1:p.Lys41Glu	CA258094 NM_001145.4:c.121A>G