Allele Registry

Canonical Allele Identifier: PA2825872019

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000482209

ClinVar Variation:

423481

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138387.1:p.Tyr292Cys	CA16618939 NM_001144915.2:c.875A>G