Canonical Allele Identifier: PA2825482981
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360661
ClinVar RCV Id: RCV000311994 RCV000369053 RCV000443075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075224.1:p.Pro674Ser
CA4293372
NM_001081755.3:c.2020C>T