Allele Registry

Canonical Allele Identifier: PA111422

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000415507

RCV000418082

RCV000425472

RCV000428300

RCV000432507

RCV000435736

RCV000786040

ClinVar Variation:

374821

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Asn549His	CA16043908 NM_000141.5:c.1645A>C