Allele Registry

Canonical Allele Identifier: PA645400432

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000488791

ClinVar Variation:

426047

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108225.1:p.Arg618Leu	CA374970924 NM_001114753.3:c.1853G>T