Canonical Allele Identifier: PA2825872965
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13280
ClinVar RCV Id: RCV000014202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138390.1:p.Ser137_Pro138delinsPheSer
CA122989
NM_001144918.2:c.410_412delinsTCT