Allele Registry

Canonical Allele Identifier: PA2827051300

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000417597

ClinVar Variation:

376153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307587.1:p.Lys657Glu	CA16602610 NM_001320658.2:c.1969A>G