Allele Registry

Canonical Allele Identifier: PA2826615836

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000272510

RCV000462325

RCV001531043

ClinVar Variation:

213171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265843.1:p.Gly99Asp	CA320313 NM_001278914.2:c.296G>A