Canonical Allele Identifier: PA2830008501
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13288
ClinVar RCV Id: RCV000014211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Asp184del
CA280189
NM_023029.2:c.551_553del