Canonical Allele Identifier: PA2828042108
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16260
ClinVar RCV Id: RCV000017648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341918.1:p.Arg1041Pro
CA257465
NM_001354989.2:c.3122G>C