Allele Registry

Canonical Allele Identifier: PA111477

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000415501

RCV001270790

RCV001591054

RCV001861462

RCV003048177

ClinVar Variation:

374818

2131381

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Cys342Gly	CA16043910 NM_000141.5:c.1024T>G CA2580082429 NM_000141.5:c.1023_1024delinsAG