Allele Registry

Canonical Allele Identifier: PA2825044641

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV001880396

ClinVar Variation:

1356315

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Asp366Asn	CA5252882 NM_000118.3:c.1096G>A