Canonical Allele Identifier: PA090999
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000007.1:p.Ser245Leu
CA220186
NM_000016.6:c.734C>T