Canonical Allele Identifier: PA915969816
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 523433
ClinVar RCV Id: RCV000626795 RCV001311284 RCV002529795
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075223.1:p.Thr305Ser
CA160131367
NM_001081754.3:c.913A>T
CA367871268
NM_001081754.3:c.914C>G