Allele Registry

Canonical Allele Identifier: PA122988

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014198

RCV000014199

RCV000224124

RCV000441051

RCV000549100

RCV000762799

RCV004532336

ClinVar Variation:

13277

HGVS (amino-acid)	Matching Registered Transcripts
NP_075259.4:p.Tyr376Cys	CA122987 NM_022970.3:c.1127A>G