Canonical Allele Identifier: PA2826031881
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 501719
ClinVar RCV Id: RCV000598386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159887.1:p.Arg537Cys
CA2738898
NM_001166415.2:c.1609C>T