Canonical Allele Identifier: PA916024565
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Asp93Ala
CA280195
NM_001320654.2:c.278A>C