Allele Registry

Canonical Allele Identifier: PA2826581487

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV001880396

ClinVar Variation:

1356315

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Asp184Asn	CA5252882 NM_001278138.2:c.550G>A