Canonical Allele Identifier: PA645380919
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374812
ClinVar RCV Id: RCV000415506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Trp290Ser
CA16043916
NM_022970.3:c.869G>C