Allele Registry

Canonical Allele Identifier: PA2830009111

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000433692

ClinVar Variation:

376727

HGVS (amino-acid)	Matching Registered Transcripts
NP_075418.1:p.Lys569Asn	CA16603135 NM_023029.2:c.1707A>T CA378314168 NM_023029.2:c.1707A>C