Allele Registry

Canonical Allele Identifier: PA658659767

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000579346

RCV002231266

RCV003989113

ClinVar Variation:

458346

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Met1Arg