Canonical Allele Identifier: PA658675572
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 449781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000492.2:p.Val154Met
CA4292496
NM_000501.4:c.460G>A