Canonical Allele Identifier: PA645500408
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 341306
ClinVar RCV Id: RCV000317019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036311.3:p.Pro17Ala
CA10651146
NM_012179.4:c.49C>G