Canonical Allele Identifier: PA915981650
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 226078
ClinVar RCV Id: RCV000211437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120800.1:p.Arg21His
CA912933
NM_001127328.3:c.62G>A