Canonical Allele Identifier: PA257469
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16265
ClinVar RCV Id: RCV000017653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_891555.2:p.Val878Met
CA257468
NM_182925.5:c.2632G>A