Allele Registry

Canonical Allele Identifier: PA2826617796

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV003518218

ClinVar Variation:

2713291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265847.1:p.Gln372Glu	CA367881956 NM_001278918.2:c.1114C>G