Allele Registry

Canonical Allele Identifier: PA2826615710

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265842.1:p.Gly539Arg	CA367889574 NM_001278913.2:c.1615G>C CA367889575 NM_001278913.2:c.1615G>A