Allele Registry

Canonical Allele Identifier: PA2826616472

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000305970

RCV000360713

RCV001551670

ClinVar Variation:

360649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265844.1:p.Gly412Arg	CA4292902 NM_001278915.2:c.1234G>A CA367881738 NM_001278915.2:c.1234G>C