Canonical Allele Identifier: PA2825061102
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320736
ClinVar RCV Id: RCV001776715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Pro423Ser
CA378326972
NM_000141.5:c.1267C>T