Canonical Allele Identifier: PA2825202578
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 523433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000492.2:p.Thr300Ser
CA160131367
NM_000501.4:c.898A>T
CA367871268
NM_000501.4:c.899C>G