Canonical Allele Identifier: PA2827050709
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Cys114Tyr
CA280168
NM_001320654.2:c.341G>A