Canonical Allele Identifier: PA2826613733
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437571
ClinVar RCV Id: RCV000503803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Gln134His
CA3933696
NM_001278716.2:c.402G>T
CA365088971
NM_001278716.2:c.402G>C