Allele Registry

Canonical Allele Identifier: PA2826700058

Gene: ACADM HGNC NCBI

ClinVar RCV:

RCV003400381

ClinVar Variation:

2633937

HGVS (amino-acid)	Matching Registered Transcripts
NP_001272971.1:p.Thr211Ser	CA340816570 NM_001286042.2:c.631A>T CA340816572 NM_001286042.2:c.632C>G