Canonical Allele Identifier: PA658812361
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 501910
ClinVar RCV Id: RCV000591304 RCV003945437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001957.2:p.Lys605Arg
CA2738917
NM_001966.4:c.1814A>G