Canonical Allele Identifier: PA916014530
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 528453
ClinVar RCV Id: RCV000633656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001272972.1:p.Tyr430Ser
CA340818359
NM_001286043.2:c.1289A>C