Canonical Allele Identifier: PA2825872502
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Ala513Thr
CA123000
NM_001144916.2:c.1537G>A