Allele Registry

Canonical Allele Identifier: PA2826581489

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000150650

RCV000309805

RCV000857857

RCV001573276

RCV002285147

RCV002453483

RCV003891683

ClinVar Variation:

163406

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Asp184His	CA295468 NM_001278138.2:c.550G>C