Canonical Allele Identifier: PA2829345731
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16260
ClinVar RCV Id: RCV000017648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002011.2:p.Arg1041Pro
CA257465
NM_002020.5:c.3122G>C