Canonical Allele Identifier: PA2827050706
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_001307583.1:p.Cys114Gly
CA16043910
NM_001320654.2:c.340T>G
CA2580082429
NM_001320654.2:c.339_340delinsAG