Canonical Allele Identifier: PA916002618
Gene: ACADVL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257376.1:p.Ala439Thr
CA251908
NM_001270447.2:c.1315G>A