Allele Registry

Canonical Allele Identifier: PA2825043978

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000455548

RCV001299080

RCV002480332

ClinVar Variation:

402828

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Val125Ala	CA5253132 NM_000118.3:c.374T>C