Canonical Allele Identifier: PA2830008527
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374812
ClinVar RCV Id: RCV000415506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Trp201Ser
CA16043916
NM_023029.2:c.602G>C