Canonical Allele Identifier: PA2825871742
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138386.1:p.Ala516Thr
CA123000
NM_001144914.1:c.1546G>A