Canonical Allele Identifier: PA2573069078
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1312158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Ala99Thr
CA4292419
NM_001278939.2:c.295G>A