Allele Registry

Canonical Allele Identifier: PA295469

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000150650

RCV000309805

RCV000857857

RCV001573276

RCV002285147

RCV002453483

RCV003891683

ClinVar Variation:

163406

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Asp366His	CA295468 NM_000118.3:c.1096G>C