Allele Registry

Canonical Allele Identifier: PA111794

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000523700

RCV001232531

ClinVar Variation:

449398

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Tyr340Cys	CA378328024 NM_000141.5:c.1019A>G