Allele Registry

Canonical Allele Identifier: PA2826616614

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265844.1:p.Gly626Arg	CA367889574 NM_001278915.2:c.1876G>C CA367889575 NM_001278915.2:c.1876G>A