Canonical Allele Identifier: PA913201530
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272972.1:p.Thr154Ile
CA252838
NM_001286043.2:c.461C>T
CA2742038349
NM_001286043.2:c.[450A>C;461C>T]