Canonical Allele Identifier: PA111381
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13298
ClinVar RCV Id: RCV000014224 RCV000414415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Ala628Thr
CA123000
NM_000141.5:c.1882G>A