Canonical Allele Identifier: PA2742036720
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 2882980
ClinVar RCV Id: RCV003763559
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995308.1:p.Phe126Leu
CA3497015
NM_205836.3:c.376T>C
CA361654874
NM_205836.3:c.378T>G
CA361654875
NM_205836.3:c.378T>A