Allele Registry

Canonical Allele Identifier: PA111768

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000415488

RCV001547058

RCV002524678

RCV004544729

ClinVar Variation:

374811

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Tyr281Cys	CA16043917 NM_000141.5:c.842A>G