Canonical Allele Identifier: PA2825061104
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393582
ClinVar RCV Id: RCV001884572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Arg426Ser
CA378326954
NM_000141.5:c.1278A>T
CA378326955
NM_000141.5:c.1278A>C