Canonical Allele Identifier: PA2826615311
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 226631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265841.1:p.Gly610Ser
CA4293247
NM_001278912.2:c.1828G>A