Canonical Allele Identifier: PA2825003229
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 934938
ClinVar RCV Id: RCV001203427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000007.1:p.Asn194Ser
CA24627682
NM_000016.6:c.581A>G