Canonical Allele Identifier: PA2826616607
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265844.1:p.Leu615Phe
CA4293244
NM_001278915.2:c.1843C>T