Canonical Allele Identifier: PA2827051136
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 478049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Ala314Ser
CA378328613
NM_001320658.2:c.940G>T