Canonical Allele Identifier: PA2825872734
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13281
ClinVar Variation Id: 13293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138389.1:p.Trp290Cys
CA122994
NM_001144917.2:c.870G>T
CA280182
NM_001144917.2:c.870G>C