Canonical Allele Identifier: PA2825061096
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576791
ClinVar RCV Id: RCV003323096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Phe409Val
CA214305295
NM_000141.5:c.1225T>G