Canonical Allele Identifier: PA2825871945
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Ala226Ser
CA122992
NM_001144915.2:c.676G>T