Canonical Allele Identifier: PA2825357797
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2730912
ClinVar RCV Id: RCV003588330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Glu139Asp
CA6152689
NM_001031847.3:c.417G>C
CA381636618
NM_001031847.3:c.417G>T