Canonical Allele Identifier: PA2825873371
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138391.1:p.Ser178Pro
CA210548
NM_001144919.2:c.532T>C