Allele Registry

Canonical Allele Identifier: PA099036

Gene: ANG HGNC NCBI

ClinVar RCV:

RCV000019707

RCV003398548

RCV003565384

ClinVar Variation:

18081

HGVS (amino-acid)	Matching Registered Transcripts
NP_001091046.1:p.Pro136Leu	CA258112 NM_001097577.3:c.407C>T