Canonical Allele Identifier: PA2825061019
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_000132.3:p.Cys342del
CA2580082428
NM_000141.5:c.1025_1027del