Allele Registry

Canonical Allele Identifier: PA2825044562

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000462769

RCV000791420

RCV001531114

RCV002379438

ClinVar Variation:

407115

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Gly331Ser	CA16612528 NM_000118.3:c.991G>A