Canonical Allele Identifier: PA220192
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 92273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Ala425Thr
CA220191
NM_000018.4:c.1273G>A