Allele Registry

Canonical Allele Identifier: PA111714

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014200

RCV000424237

RCV001382546

ClinVar Variation:

13278

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Ser372Cys	CA256747 NM_000141.5:c.1115C>G