Allele Registry

Canonical Allele Identifier: PA2825044338

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000633133

ClinVar Variation:

528053

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Thr233Met	CA5253010 NM_000118.3:c.698C>T