Canonical Allele Identifier: PA100756
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 96711
ClinVar RCV Id: RCV000082871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001957.2:p.Glu3Lys
CA149692
NM_001966.4:c.7G>A