Canonical Allele Identifier: PA916014415
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 226062
ClinVar Variation Id: 281055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272972.1:p.Lys177del
CA913102
NM_001286043.2:c.529_531del
CA10603794
NM_001286043.2:c.522_524del
CA340812883
NM_001286043.2:c.523A>T
CA340812893
NM_001286043.2:c.526A>T
CA340812902
NM_001286043.2:c.529A>T