Allele Registry

Canonical Allele Identifier: PA2826581552

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000018154

ClinVar Variation:

16674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Gly231Val	CA257572 NM_001278138.2:c.692G>T