Allele Registry

Canonical Allele Identifier: PA202697

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000148486

RCV000178045

RCV000346221

RCV000857942

RCV001258238

RCV001588996

RCV002371988

ClinVar Variation:

161232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Pro131Leu	CA202695 NM_001114753.3:c.392C>T