Canonical Allele Identifier: PA658800012
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 502112
ClinVar RCV Id: RCV000596994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Val109Glu
CA397722591
NM_000018.4:c.326T>A