Canonical Allele Identifier: PA2826615956
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 523433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Thr295Ser
CA160131367
NM_001278914.2:c.883A>T
CA367871268
NM_001278914.2:c.884C>G