Allele Registry

Canonical Allele Identifier: PA111618

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000415486

RCV000655413

RCV001723974

ClinVar Variation:

374809

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Phe276Val	CA16043919 NM_000141.5:c.826T>G