Canonical Allele Identifier: PA658812364
Gene: EHHADH HGNC NCBI

Linked Data

ClinVar Variation Id: 501017
ClinVar RCV Id: RCV000594486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001957.2:p.Val675Ile
CA355675515
NM_001966.4:c.2023G>A