Canonical Allele Identifier: PA2827050690
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29854
ClinVar RCV Id: RCV000022733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ala109Thr
CA128691
NM_001320654.2:c.325G>A