Allele Registry

Canonical Allele Identifier: PA658697544

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000488736

RCV000757217

ClinVar Variation:

426042

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Ile263Asn	CA374983163 NM_001114753.3:c.788T>A