Canonical Allele Identifier: PA916002680
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 1632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257376.1:p.Phe481Leu
CA251907
NM_001270447.2:c.1441T>C
CA397724980
NM_001270447.2:c.1443C>G
CA397724981
NM_001270447.2:c.1443C>A