Canonical Allele Identifier: PA2826031891
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 501017
ClinVar RCV Id: RCV000594486
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159887.1:p.Val579Ile
CA355675515
NM_001166415.2:c.1735G>A