Canonical Allele Identifier: PA2825602978
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 226062
ClinVar RCV Id: RCV000211510 RCV000313722
ClinVar Variation Id: 281055
ClinVar RCV Id: RCV000297824 RCV001242051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120800.1:p.Lys148del
CA913102
NM_001127328.3:c.442_444del
CA10603794
NM_001127328.3:c.435_437del
CA340812883
NM_001127328.3:c.436A>T
CA340812893
NM_001127328.3:c.439A>T
CA340812902
NM_001127328.3:c.442A>T