Canonical Allele Identifier: PA2825872351
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374818
ClinVar Variation Id: 2131381
ClinVar RCV Id: RCV003048177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Cys227Gly
CA16043910
NM_001144916.2:c.679T>G
CA2580082429
NM_001144916.2:c.678_679delinsAG