Canonical Allele Identifier: PA2825871653
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393582
ClinVar RCV Id: RCV001884572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138386.1:p.Arg314Ser
CA378326954
NM_001144914.1:c.942A>T
CA378326955
NM_001144914.1:c.942A>C