Canonical Allele Identifier: PA915957728
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 474895
ClinVar RCV Id: RCV000541584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001029031.1:p.Phe91Leu
CA397722613
NM_001033859.2:c.271T>C
CA397722617
NM_001033859.2:c.273C>A
CA397722618
NM_001033859.2:c.273C>G