Allele Registry

Canonical Allele Identifier: PA111688

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000014208

RCV000014209

RCV000256107

RCV000415503

RCV000528973

RCV003313920

ClinVar Variation:

13286

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Ser351Cys	CA122991 NM_000141.5:c.1052C>G