Allele Registry

Canonical Allele Identifier: PA645510374

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000508217

RCV001370738

ClinVar Variation:

439648

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Ala243Thr	CA5253001 NM_001114753.3:c.727G>A