Canonical Allele Identifier: PA916028425
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8954
ClinVar RCV Id: RCV000009511 RCV000009512 RCV000202440 RCV000440440 RCV000762941 RCV000735345 RCV003473063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Pro50His
CA254606
NM_001330589.2:c.149C>A