Canonical Allele Identifier: PA2825871452
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376315
ClinVar RCV Id: RCV000426084 RCV000420097 RCV000432646 RCV000436783 RCV000444404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138385.1:p.Asn639Lys
CA16602761
NM_001144913.1:c.1917T>A
CA378314786
NM_001144913.1:c.1917T>G