Canonical Allele Identifier: PA2828042141
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16262
ClinVar RCV Id: RCV000017650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341918.1:p.Pro1114Leu
CA257467
NM_001354989.2:c.3341C>T