Canonical Allele Identifier: PA2826618257
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 449781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Val154Met
CA4292496
NM_001278939.2:c.460G>A