Canonical Allele Identifier: PA2825871448
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138385.1:p.Ala629Thr
CA123000
NM_001144913.1:c.1885G>A