Canonical Allele Identifier: PA2826031872
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 501138
ClinVar RCV Id: RCV000598312 RCV000969464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159887.1:p.Arg506Gln
CA2738920
NM_001166415.2:c.1517G>A