Canonical Allele Identifier: PA220182
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3594
ClinVar RCV Id: RCV000003777 RCV000077891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120800.1:p.Gly199Arg
CA220181
NM_001127328.3:c.595G>A
CA340815426
NM_001127328.3:c.595G>C