Canonical Allele Identifier: PA658809777
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 497484
ClinVar RCV Id: RCV000592272 RCV001302577 RCV002245031 RCV002483578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Ala97Thr
CA5721181
NM_022970.3:c.289G>A