Canonical Allele Identifier: PA2827050717
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ser119Cys
CA280173
NM_001320654.2:c.356C>G