Canonical Allele Identifier: PA220190
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 92271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Phe369Ser
CA220189
NM_000018.4:c.1106T>C