Canonical Allele Identifier: PA2827050859
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ala400Thr
CA123000
NM_001320654.2:c.1198G>A