Allele Registry

Canonical Allele Identifier: PA2826617668

Gene: ELN HGNC NCBI

ClinVar Allele:

209919

ClinVar RCV:

RCV000198008

RCV000279620

RCV000334634

ClinVar Variation:

213175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265847.1:p.Pro176Leu	CA322484 NM_001278918.2:c.527C>T