Allele Registry

Canonical Allele Identifier: PA658659874

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV002231258

ClinVar Variation:

458331

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Ser407Asn	CA374978426 NM_001114753.3:c.1220G>A