Canonical Allele Identifier: PA2830005318
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316322
ClinVar RCV Id: RCV001766228 RCV002488617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Gly261Arg
CA378331011
NM_022970.3:c.781G>C
CA378331012
NM_022970.3:c.781G>A