Allele Registry

Canonical Allele Identifier: PA916009936

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000148487

RCV000457880

RCV000488867

RCV000859971

RCV003298151

RCV003407567

ClinVar Variation:

161233

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Gly32Ser	CA211422 NM_001278138.2:c.94G>A