Allele Registry

Canonical Allele Identifier: PA2826617514

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000298998

RCV000407993

RCV001198806

RCV004544697

ClinVar Variation:

360660

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265846.1:p.Ala627Thr	CA4293282 NM_001278917.2:c.1879G>A