Allele Registry

Canonical Allele Identifier: PA916009957

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000508217

RCV001370738

ClinVar Variation:

439648

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Ala61Thr	CA5253001 NM_001278138.2:c.181G>A