Allele Registry

Canonical Allele Identifier: PA645381049

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000417871

RCV000424365

RCV000435530

ClinVar Variation:

376162

376163

376164

HGVS (amino-acid)	Matching Registered Transcripts
NP_075259.4:p.Met536Ile	CA16602619 NM_022970.3:c.1608G>T CA16602620 NM_022970.3:c.1608G>C CA16602621 NM_022970.3:c.1608G>A