Canonical Allele Identifier: PA2830008708
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2093701
ClinVar RCV Id: RCV002996861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Cys253del
CA378327957
NM_023029.2:c.759C>A
CA2580082428
NM_023029.2:c.758_760del