Canonical Allele Identifier: PA658812363
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 501719
ClinVar RCV Id: RCV000598386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001957.2:p.Arg633Cys
CA2738898
NM_001966.4:c.1897C>T