Canonical Allele Identifier: PA2830008835
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393582
ClinVar RCV Id: RCV001884572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Arg337Ser
CA378326954
NM_023029.2:c.1011A>T
CA378326955
NM_023029.2:c.1011A>C