Allele Registry

Canonical Allele Identifier: PA2826616931

Gene: ELN HGNC NCBI

ClinVar Allele:

567112

ClinVar RCV:

RCV000689870

RCV001551083

ClinVar Variation:

569280

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265845.1:p.Gly408Arg	CA367881796 NM_001278916.2:c.1222G>C