Allele Registry

Canonical Allele Identifier: PA2825482063

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001551555

RCV002570692

RCV004528513

ClinVar Variation:

1190736

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075222.1:p.Gly433Arg	CA4292916 NM_001081753.3:c.1297G>A CA367881828 NM_001081753.3:c.1297G>C