Canonical Allele Identifier: PA2573299391
Gene: RFT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1391388
ClinVar RCV Id: RCV001893051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443091.1:p.Ser80Arg
CA353222568
NM_052859.4:c.240C>G
CA353222569
NM_052859.4:c.240C>A
CA353222575
NM_052859.4:c.238A>C