Canonical Allele Identifier: PA111741
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13281
ClinVar RCV Id: RCV000014203 RCV000419759 RCV002254264 RCV003150929 RCV004532337
ClinVar Variation Id: 13293
ClinVar RCV Id: RCV000014217 RCV000014218 RCV000655418 RCV001268882 RCV002490362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Trp290Cys
CA122994
NM_000141.5:c.870G>T
CA280182
NM_000141.5:c.870G>C