Canonical Allele Identifier: PA2573070736
Gene: HADH HGNC NCBI

Linked Data

ClinVar Variation Id: 212734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317956.2:p.Tyr230His
CA207951
NM_001331027.2:c.688T>C