Canonical Allele Identifier: PA2825873519
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138391.1:p.Glu477Ala
CA280192
NM_001144919.2:c.1430A>C