Canonical Allele Identifier: PA2826157103
Gene: FBXO11 HGNC NCBI

Linked Data

ClinVar Variation Id: 559601
ClinVar RCV Id: RCV000677378 RCV001291313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177203.1:p.Arg138Ser
CA346813373
NM_001190274.2:c.414A>C
CA346813374
NM_001190274.2:c.414A>T