Canonical Allele Identifier: PA106687
Gene: FLT4 HGNC NCBI
ClinVar RCV:
RCV000017648
ClinVar Variation:
16260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_891555.2:p.Arg1041Pro
CA257465
NM_182925.5:c.3122G>C