Canonical Allele Identifier: PA2826700098
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 3588
ClinVar RCV Id: RCV000003771 RCV000185665 RCV003415641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272971.1:p.Gly231Arg
CA252824
NM_001286042.2:c.691G>A
CA340816708
NM_001286042.2:c.691G>C