Canonical Allele Identifier: PA2826617544
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265846.1:p.Pro683Ser
CA4293372
NM_001278917.2:c.2047C>T