Allele Registry

Canonical Allele Identifier: PA2825871999

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV003028849

ClinVar Variation:

2103395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138387.1:p.Trp267Gly	CA378327672 NM_001144915.2:c.799T>G