Canonical Allele Identifier: PA2826700056
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272971.1:p.Ser209Leu
CA220186
NM_001286042.2:c.626C>T