Canonical Allele Identifier: PA2828042071
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16259
ClinVar RCV Id: RCV000017647 RCV003441720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341918.1:p.Gly857Arg
CA257464
NM_001354989.2:c.2569G>A
CA362501839
NM_001354989.2:c.2569G>C