Allele Registry

Canonical Allele Identifier: PA658803095

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV002234424

ClinVar Variation:

528069

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Pro225Ala	CA374983508 NM_001114753.3:c.673C>G