Canonical Allele Identifier: PA252835
Gene: ACADM HGNC NCBI
ClinVar Allele:
18635
ClinVar RCV:
RCV000003779
ClinVar Variation:
3596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120800.1:p.Arg285Thr
CA252834
NM_001127328.3:c.854G>C