Allele Registry

Canonical Allele Identifier: PA2826581697

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000226902

RCV000454429

RCV000488732

RCV000664173

RCV001166478

RCV002225526

RCV002399808

ClinVar Variation:

237022

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Gly363Ser	CA5252712 NM_001278138.2:c.1087G>A