Canonical Allele Identifier: PA658661980
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Phe87Leu
CA4292410
NM_001278939.2:c.259T>C
CA367869203
NM_001278939.2:c.261T>A
CA367869204
NM_001278939.2:c.261T>G