Allele Registry

Canonical Allele Identifier: PA2826617891

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265847.1:p.Gly531Arg	CA367889574 NM_001278918.2:c.1591G>C CA367889575 NM_001278918.2:c.1591G>A