Canonical Allele Identifier: PA2826700505
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 2448116
ClinVar RCV Id: RCV003181480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272972.1:p.Thr42Ser
CA340809097
NM_001286043.2:c.124A>T
CA340809101
NM_001286043.2:c.125C>G