Canonical Allele Identifier: PA2826142527
Gene: HADH HGNC NCBI

Linked Data

ClinVar Variation Id: 212734
ClinVar RCV Id: RCV000194052 RCV001762415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171634.3:p.Tyr226His
CA207951
NM_001184705.4:c.676T>C