Allele Registry

Canonical Allele Identifier: PA2827051299

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000433692

ClinVar Variation:

376727

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307587.1:p.Lys656Asn	CA16603135 NM_001320658.2:c.1968A>T CA378314168 NM_001320658.2:c.1968A>C