Allele Registry

Canonical Allele Identifier: PA2830008787

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000482209

ClinVar Variation:

423481

HGVS (amino-acid)	Matching Registered Transcripts
NP_075418.1:p.Tyr292Cys	CA16618939 NM_023029.2:c.875A>G