Allele Registry

Canonical Allele Identifier: PA2826581779

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000999220

RCV001069948

RCV002481795

ClinVar Variation:

810423

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Thr435Met	CA5252620 NM_001278138.2:c.1304C>T