Allele Registry

Canonical Allele Identifier: PA111802

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014175

RCV001214882

RCV001723564

ClinVar Variation:

13264

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Tyr340His	CA280169 NM_000141.5:c.1018T>C