Allele Registry

Canonical Allele Identifier: PA111697

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014176

RCV000623131

RCV000655419

RCV001565300

RCV002287333

ClinVar Variation:

13265

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Ser354Cys	CA280170 NM_000141.5:c.1061C>G