Canonical Allele Identifier: PA122990
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_075259.4:p.Ser252_Pro253delinsPheSer
CA122989
NM_022970.3:c.755_757delinsTCT