Allele Registry

Canonical Allele Identifier: PA258102

Gene: ANG HGNC NCBI

ClinVar Allele:

33116

ClinVar RCV:

RCV000019703

ClinVar Variation:

18077

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136.1:p.Cys63Trp	CA258100 NM_001145.4:c.189C>G