Canonical Allele Identifier: PA2825872293
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13281
ClinVar Variation Id: 13293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Trp175Cys
CA122994
NM_001144916.2:c.525G>T
CA280182
NM_001144916.2:c.525G>C