Canonical Allele Identifier: PA2825872837
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138389.1:p.Ala512Thr
CA123000
NM_001144917.2:c.1534G>A