Allele Registry

Canonical Allele Identifier: PA916069505

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000121066

RCV000390607

RCV000417413

RCV000543983

RCV001103686

RCV001105633

RCV001105634

RCV001105635

ClinVar Variation:

134392

HGVS (amino-acid)	Matching Registered Transcripts
NP_075418.1:p.Met97Thr	CA159675 NM_023029.2:c.290T>C