Canonical Allele Identifier: PA106705
Gene: FLT4 HGNC NCBI
ClinVar RCV:
RCV000017651
ClinVar Variation:
16263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_891555.2:p.His1035Arg
CA126342
NM_182925.5:c.3104A>G