Canonical Allele Identifier: PA2828503133
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_001361254.1:p.Arg54Ser
CA346813373
NM_001374325.1:c.162A>C
CA346813374
NM_001374325.1:c.162A>T