Canonical Allele Identifier: PA916028430
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 203666
ClinVar RCV Id: RCV000440638 RCV001085585 RCV001804920 RCV003947559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Asp118Gly
CA312436
NM_001330589.2:c.353A>G