Canonical Allele Identifier: PA2830008461
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13279
ClinVar RCV Id: RCV000014201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Ser163Phe
CA280180
NM_023029.2:c.488_489delinsTT