Allele Registry

Canonical Allele Identifier: PA098988

Gene: ANG HGNC NCBI

ClinVar RCV:

RCV000019699

ClinVar Variation:

18073

HGVS (amino-acid)	Matching Registered Transcripts
NP_001091046.1:p.Gln36Leu	CA258088 NM_001097577.3:c.107A>T