Canonical Allele Identifier: PA2825067625
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423479
ClinVar RCV Id: RCV001928870 RCV002479443 RCV002558486 RCV003452176 RCV003452177 RCV003452178 RCV003452175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Gly375Val
CA859131
NM_000098.3:c.1124G>T