Canonical Allele Identifier: PA2826616403
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 523433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265844.1:p.Thr300Ser
CA160131367
NM_001278915.2:c.898A>T
CA367871268
NM_001278915.2:c.899C>G