Canonical Allele Identifier: PA2825871951
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Asp232Ala
CA280195
NM_001144915.2:c.695A>C