Canonical Allele Identifier: PA645489700
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 226061
ClinVar RCV Id: RCV000211487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000007.1:p.Tyr353Asp
CA10576243
NM_000016.6:c.1057T>G