Canonical Allele Identifier: PA658675390
Gene: ACADVL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Ser418Asn
CA397724694
NM_000018.4:c.1253G>A