Allele Registry

Canonical Allele Identifier: PA916009947

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000633133

ClinVar Variation:

528053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Thr51Met	CA5253010 NM_001278138.2:c.152C>T