Canonical Allele Identifier: PA2830008741
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Ser262Cys
CA122991
NM_023029.2:c.785C>G