Allele Registry

Canonical Allele Identifier: PA2826615117

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000627826

ClinVar Variation:

524218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265841.1:p.Lys315Arg	CA367871485 NM_001278912.2:c.944A>G