Allele Registry

Canonical Allele Identifier: PA2826581436

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000462769

RCV000791420

RCV001531114

RCV002379438

ClinVar Variation:

407115

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Gly149Ser	CA16612528 NM_001278138.2:c.445G>A