Allele Registry

Canonical Allele Identifier: PA2826701129

Gene: ACADM HGNC NCBI

ClinVar RCV:

RCV000211450

ClinVar Variation:

226065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001272973.1:p.Leu14Phe	CA10576236 NM_001286044.2:c.42A>C CA340815810 NM_001286044.2:c.42A>T