Canonical Allele Identifier: PA2826031846
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 501508
ClinVar RCV Id: RCV000596768
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159887.1:p.Val376Leu
CA355677564
NM_001166415.2:c.1126G>C