Canonical Allele Identifier: PA312269
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 21013
ClinVar RCV Id: RCV000020069 RCV002514121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Thr409Met
CA312268
NM_000018.4:c.1226C>T