Canonical Allele Identifier: PA1139725657
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 844640
ClinVar RCV Id: RCV001047545 RCV003145287 RCV003455197 RCV003455198 RCV003455199 RCV003455200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Met438Val
CA859173
NM_001330589.2:c.1312A>G