Canonical Allele Identifier: PA2828042170
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3048685
ClinVar RCV Id: RCV003956681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341918.1:p.Gly1238Trp
CA362498069
NM_001354989.2:c.3712G>T