Canonical Allele Identifier: PA111794
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Tyr340Cys
CA378328024
NM_000141.5:c.1019A>G