Allele Registry

Canonical Allele Identifier: PA916009968

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000488736

RCV000757217

ClinVar Variation:

426042

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Ile81Asn	CA374983163 NM_001278138.2:c.242T>A