Allele Registry

Canonical Allele Identifier: PA122995

Gene: FGFR2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000014203

RCV000014217

RCV000014218

RCV000419759

RCV000655418

RCV001268882

RCV002254264

RCV002490362

RCV003150929

RCV004532337

ClinVar Variation:

13281

13293

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_075259.4:p.Trp290Cys	CA122994 NM_022970.3:c.870G>T CA280182 NM_022970.3:c.870G>C