Allele Registry

Canonical Allele Identifier: PA2825482930

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075224.1:p.Gly601Arg	CA367889574 NM_001081755.3:c.1801G>C CA367889575 NM_001081755.3:c.1801G>A