Allele Registry

Canonical Allele Identifier: PA2826581321

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV001764537

RCV002231269

ClinVar Variation:

458349

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Thr11Met	CA5253082 NM_001278138.2:c.32C>T