Allele Registry

Canonical Allele Identifier: PA2573069031

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV001803611

ClinVar Variation:

1330519

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Ile81Ser	CA374983166 NM_001278138.2:c.242T>G