Canonical Allele Identifier: PA240065
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 194201
ClinVar RCV Id: RCV000174513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Met489Ile
CA240064
NM_001031847.3:c.1467G>A
CA381630107
NM_001031847.3:c.1467G>T
CA381630109
NM_001031847.3:c.1467G>C