Canonical Allele Identifier: PA2826699806
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3591
ClinVar Variation Id: 226059
ClinVar RCV Id: RCV000211526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272971.1:p.Met113Ile
CA252830
NM_001286042.2:c.339G>A
CA913107
NM_001286042.2:c.339G>T
CA340812971
NM_001286042.2:c.339G>C