Canonical Allele Identifier: PA1139751693
Gene: RFT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 902912
ClinVar RCV Id: RCV001149815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443091.1:p.Thr75Ile
CA353222606
NM_052859.4:c.224C>T