Canonical Allele Identifier: PA2827051285
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Ala626Thr
CA123000
NM_001320658.2:c.1876G>A