Allele Registry

Canonical Allele Identifier: PA658659876

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000547986

RCV002367790

ClinVar Variation:

458332

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Cys412Tyr	CA374978391 NM_001114753.3:c.1235G>A