Canonical Allele Identifier: PA2573284372
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393582
ClinVar RCV Id: RCV001884572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Arg427Ser
CA378326954
NM_022970.3:c.1281A>T
CA378326955
NM_022970.3:c.1281A>C