Canonical Allele Identifier: PA111673
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13290
ClinVar RCV Id: RCV000014213 RCV000435703 RCV000408850 RCV000690962 RCV002508123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Ser267Pro
CA210548
NM_000141.5:c.799T>C