Canonical Allele Identifier: PA091002
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3595
ClinVar RCV Id: RCV000003778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000007.1:p.Thr193Ala
CA252832
NM_000016.6:c.577A>G