Canonical Allele Identifier: PA2580553901
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2270022
ClinVar RCV Id: RCV002804458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_891555.2:p.Pro1262Ser
CA362497914
NM_182925.5:c.3784C>T