Canonical Allele Identifier: PA916024585
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Ala344Gly
CA280171
NM_001320658.2:c.1031C>G