Canonical Allele Identifier: PA2825871950
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060632
ClinVar RCV Id: RCV001370090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Asp232Val
CA378328475
NM_001144915.2:c.695A>T