Canonical Allele Identifier: PA2825872392
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 478046
ClinVar RCV Id: RCV000525216 RCV000762798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Gly269Arg
CA378327226
NM_001144916.2:c.805G>A
CA378327227
NM_001144916.2:c.805G>C