Allele Registry

Canonical Allele Identifier: PA2825481729

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075221.1:p.Gly591Arg	CA367889574 NM_001081752.3:c.1771G>C CA367889575 NM_001081752.3:c.1771G>A