Canonical Allele Identifier: PA2741889899
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2530245
ClinVar RCV Id: RCV003290864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Gly152Ser
CA381636153
NM_001876.4:c.454G>A