Canonical Allele Identifier: PA916014552
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3595
ClinVar RCV Id: RCV000003778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272973.1:p.Thr4Ala
CA252832
NM_001286044.2:c.10A>G