Canonical Allele Identifier: PA2830009081
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Ala539Thr
CA123000
NM_023029.2:c.1615G>A