Canonical Allele Identifier: PA220222
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 92291
ClinVar RCV Id: RCV000077924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Ala263Thr
CA220221
NM_000018.4:c.787G>A