Canonical Allele Identifier: PA645467814
Gene: CBLIF HGNC NCBI

Linked Data

ClinVar Variation Id: 305043
ClinVar RCV Id: RCV000326236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005133.2:p.Lys73Arg
CA6021653
NM_005142.2:c.218A>G