Allele Registry

Canonical Allele Identifier: PA111467

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014177

RCV000014178

RCV000014179

RCV000014180

RCV000534888

RCV001723565

ClinVar Variation:

13266

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Cys342Arg	CA256745 NM_000141.5:c.1024T>C