Canonical Allele Identifier: PA2826617718
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 523433
ClinVar RCV Id: RCV000626795 RCV001311284 RCV002529795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265847.1:p.Thr256Ser
CA160131367
NM_001278918.2:c.766A>T
CA367871268
NM_001278918.2:c.767C>G