Allele Registry

Canonical Allele Identifier: PA2825044435

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV001803611

ClinVar Variation:

1330519

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Ile263Ser	CA374983166 NM_000118.3:c.788T>G