Canonical Allele Identifier: PA2580493762
Gene: RFT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2089939
ClinVar RCV Id: RCV003005729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443091.1:p.Thr58Asn
CA2451515
NM_052859.4:c.173C>A