Allele Registry

Canonical Allele Identifier: PA111788

Gene: FGFR2 HGNC NCBI

ClinVar Allele:

28309

ClinVar RCV:

RCV000014189

RCV000798719

ClinVar Variation:

13270

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Tyr328Cys	CA280172 NM_000141.5:c.983A>G