Canonical Allele Identifier: PA111722
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Thr341Pro
CA280176
NM_000141.5:c.1021A>C