Canonical Allele Identifier: PA658800016
Gene: ACADVL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Leu144Pro
CA397722889
NM_000018.4:c.431T>C