Canonical Allele Identifier: PA891850544
Gene: ACADSB HGNC NCBI

Linked Data

ClinVar Variation Id: 571020
ClinVar RCV Id: RCV000692041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001600.1:p.Asp59Gly
CA378616108
NM_001609.3:c.176A>G