Allele Registry

Canonical Allele Identifier: PA2499245010

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265868.1:p.Gly682Arg	CA367889574 NM_001278939.2:c.2044G>C CA367889575 NM_001278939.2:c.2044G>A