Canonical Allele Identifier: PA2825871342
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138385.1:p.Met392Arg
CA128693
NM_001144913.1:c.1175T>G