Canonical Allele Identifier: PA2830008543
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2852948
ClinVar RCV Id: RCV003754764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Pro214Arg
CA214312758
NM_023029.2:c.641C>G
CA645568656
NM_023029.2:c.641_642delinsGT