Canonical Allele Identifier: PA916002579
Gene: ACADVL HGNC NCBI
ClinVar RCV:
RCV000652042
ClinVar Variation:
203581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257376.1:p.Phe399Ser
CA312266
NM_001270447.2:c.1196T>C