Canonical Allele Identifier: PA106698
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16259
ClinVar RCV Id: RCV000017647 RCV003441720
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_891555.2:p.Gly857Arg
CA257464
NM_182925.5:c.2569G>A
CA362501839
NM_182925.5:c.2569G>C