Canonical Allele Identifier: PA915957721
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 21022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001029031.1:p.Leu17Phe
CA341522
NM_001033859.2:c.49C>T