Canonical Allele Identifier: PA126349
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16276
ClinVar RCV Id: RCV000017666 RCV000017665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004110.2:p.Asp835Tyr
CA126347
NM_004119.3:c.2503G>T