Canonical Allele Identifier: PA645380874
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_075259.4:p.Val269_Val270del
CA10575516
NM_022970.3:c.804_809del