Canonical Allele Identifier: PA916028417
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 556806
ClinVar RCV Id: RCV000672860 RCV002499183 RCV002532136 RCV003453357 RCV003456125 RCV003453358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Gly13del
CA658821045
NM_001330589.2:c.37_39del