Canonical Allele Identifier: PA2825872356
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Ala229Gly
CA280171
NM_001144916.2:c.686C>G