Canonical Allele Identifier: PA2828042172
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2246059
ClinVar RCV Id: RCV002776712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341918.1:p.Arg1251Ser
CA3605705
NM_001354989.2:c.3753G>T
CA362497988
NM_001354989.2:c.3753G>C