Canonical Allele Identifier: PA2826699791
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 226062
ClinVar Variation Id: 281055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272971.1:p.Lys108del
CA913102
NM_001286042.2:c.322_324del
CA10603794
NM_001286042.2:c.315_317del
CA340812883
NM_001286042.2:c.316A>T
CA340812893
NM_001286042.2:c.319A>T
CA340812902
NM_001286042.2:c.322A>T