Canonical Allele Identifier: PA916024564
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ala87Ser
CA122992
NM_001320654.2:c.259G>T