Canonical Allele Identifier: PA2825061298
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13297
ClinVar RCV Id: RCV000014223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Arg649_Asp650delinsSer
CA10575519
NM_000141.5:c.1947_1949del