Allele Registry

Canonical Allele Identifier: PA111722

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014194

RCV001037961

RCV001781263

ClinVar Variation:

13274

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Thr341Pro	CA280176 NM_000141.5:c.1021A>C