Canonical Allele Identifier: PA658800019
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 501313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Phe192Ser
CA397723196
NM_000018.4:c.575T>C