Canonical Allele Identifier: PA2825357793
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2144150
ClinVar RCV Id: RCV003068249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Gly134Arg
CA6152692
NM_001031847.3:c.400G>A
CA381636657
NM_001031847.3:c.400G>C