Canonical Allele Identifier: PA095994
Gene: RFT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443091.1:p.Arg67Cys
CA251606
NM_052859.4:c.199C>T