Canonical Allele Identifier: PA2827050700
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Thr113Pro
CA280176
NM_001320654.2:c.337A>C