Allele Registry

Canonical Allele Identifier: PA2826581643

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV001084927

RCV003640900

RCV003970317

ClinVar Variation:

414304

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Val301Ile	CA5252756 NM_001278138.2:c.901G>A