Canonical Allele Identifier: PA2827050868
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13297
ClinVar RCV Id: RCV000014223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Arg421_Asp422delinsSer
CA10575519
NM_001320654.2:c.1263_1265del