Canonical Allele Identifier: PA2830008570
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13289
ClinVar RCV Id: RCV000014212 RCV000856813 RCV001280733 RCV001851847 RCV002496355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Ala226Ser
CA122992
NM_023029.2:c.676G>T