Canonical Allele Identifier: PA2573299385
Gene: RFT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1409672
ClinVar RCV Id: RCV001939891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443091.1:p.Leu61Pro
CA2451513
NM_052859.4:c.182T>C