Allele Registry

Canonical Allele Identifier: PA2826581599

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000633145

RCV001285345

RCV002385994

RCV003480725

ClinVar Variation:

528065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Val258Gly	CA374977914 NM_001278138.2:c.773T>G