Allele Registry

Canonical Allele Identifier: PA111813

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014198

RCV000014199

RCV000224124

RCV000441051

RCV000549100

RCV000762799

RCV004532336

ClinVar Variation:

13277

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Tyr375Cys	CA122987 NM_000141.5:c.1124A>G