Allele Registry

Canonical Allele Identifier: PA916009939

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV002234424

ClinVar Variation:

528069

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Pro43Ala	CA374983508 NM_001278138.2:c.127C>G