Canonical Allele Identifier: PA2830009106
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1285493
ClinVar RCV Id: RCV001706850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Ile565Val
CA5720605
NM_023029.2:c.1693A>G