Allele Registry

Canonical Allele Identifier: PA295809

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000155541

RCV000284602

RCV001083206

RCV001573847

RCV002390352

ClinVar Variation:

178774

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Thr5Met	CA295808 NM_000118.3:c.14C>T