Canonical Allele Identifier: PA2825872269
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13285
ClinVar RCV Id: RCV000014207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Val154_Val155del
CA10575516
NM_001144916.2:c.459_464del