Canonical Allele Identifier: PA2825871883
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13280
ClinVar RCV Id: RCV000014202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Ser163_Pro164delinsPheSer
CA122989
NM_001144915.2:c.488_490delinsTCT